71 results
Allele/Variant Genes: H2-K1 (Mmu) Molecular Consequence: 3 prime UTR variant
Allele/Variant
Source: rs214064625
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215136T>C

Allele/Variant
Source: rs108517543
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215177C>A

Allele/Variant
Source: rs1134898098
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215580A>G

Allele/Variant
Source: rs236786216
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215596A>C

Allele/Variant
Source: rs215027887
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215052A>T

Allele/Variant
Source: rs108899167
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215260G>C

Allele/Variant
Source: rs262090929
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215266G>A

Allele/Variant
Source: rs52023780
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215403A>T

Allele/Variant
Source: rs214684025
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215412T>A

Allele/Variant
Source: rs33335732
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215486A>T

Allele/Variant
Source: rs584215592
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215162G>A

Allele/Variant
Source: rs47766739
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215218T>C

Allele/Variant
Source: rs583991945
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215352C>G

Allele/Variant
Source: rs587009654
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215449C>T

Allele/Variant
Source: rs255474640
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215611G>T

Allele/Variant
Source: rs1132602514
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215626A>T

Allele/Variant
Source: rs253663873
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215117A>C

Allele/Variant
Source: rs33490761
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215587C>T

Allele/Variant
Source: rs46365172
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215672A>G

Allele/Variant
Source: rs244180327
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215270T>C

Allele/Variant
Source: rs215838515
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215174T>C

Allele/Variant
Source: rs108185637
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215450G>A

Allele/Variant
Source: rs1132979433
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215628C>T

Allele/Variant
Source: rs864256776
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215699A>C

Allele/Variant
Source: rs231523510
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215300G>A

Allele/Variant
Source: rs264909002
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215329G>A

Allele/Variant
Source: rs584479214
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215550G>A

Allele/Variant
Source: rs234422264
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215240A>C

Allele/Variant
Source: rs50907505
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215284C>G

Allele/Variant
Source: rs248972806
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215331C>G

Allele/Variant
Source: rs1133365110
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215610A>T

Allele/Variant
Source: rs580616236
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215249G>A

Allele/Variant
Source: rs108359379
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215431T>A

Allele/Variant
Source: rs581368343
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215476C>T

Allele/Variant
Source: rs1134795940
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215533T>C

Allele/Variant
Source: rs221191123
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215620T>A

Allele/Variant
Source: rs108878265
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215700C>A

Allele/Variant
Source: rs234445566
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215118G>A

Allele/Variant
Source: rs29520363
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215346G>T

Allele/Variant
Source: rs51588245
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215359T>A

Allele/Variant
Source: rs257035173
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215040C>A

Allele/Variant
Source: rs1134327243
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215575A>C

Allele/Variant
Source: rs214684025
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215412T>C

Allele/Variant
Source: rs1134433098
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215520G>T

Allele/Variant
Source: rs244718821
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215138C>T

Allele/Variant
Source: rs107824902
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215293G>C

Allele/Variant
Source: rs241486979
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215324A>T

Allele/Variant
Source: rs108754451
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215379G>T

Allele/Variant
Source: rs1132882623
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215556A>G

Allele/Variant
Source: rs1133760371
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, splice_donor_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215588A>G