2,550 results
Allele/Variant Genes: Gm28539 (Mmu)
Allele/Variant
Source: rs216263650
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18655446C>T

Allele/Variant
Source: rs218861296
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18655737T>C

Allele/Variant
Source: rs261986128
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660454C>T

Allele/Variant
Source: rs216868718
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660536A>G

Allele/Variant
Source: rs228248054
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660571A>G

Allele/Variant
Source: rs214715164
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660690G>A

Allele/Variant
Source: rs227701746
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18662629C>T

Allele/Variant
Source: rs244508418
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18657517G>A

Allele/Variant
Source: rs217045826
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18678298C>T

Allele/Variant
Source: rs234446352
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18678359T>C

Allele/Variant
Source: rs258196320
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18685424T>A

Allele/Variant
Source: rs239349071
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18689184T>C

Allele/Variant
Source: rs254902675
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18690402T>G

Allele/Variant
Source: rs248809660
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18690758A>G

Allele/Variant
Source: rs260433774
Genes: Gm28539 (Mmu), Mrpl40 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18694063C>T

Allele/Variant
Source: rs211885489
Genes: Gm28539 (Mmu), Mrpl40 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18692579C>T

Allele/Variant
Source: rs248436023
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18696987C>T

Allele/Variant
Source: rs265508755
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18697398C>T

Allele/Variant
Source: rs226896946
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18697431C>G

Allele/Variant
Source: rs219591177
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18697538C>A

Allele/Variant
Source: rs248936417
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18655734G>C

Allele/Variant
Source: rs220668660
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660129G>A

Allele/Variant
Source: rs237648667
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660153T>C

Allele/Variant
Source: rs248144785
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660219A>G

Allele/Variant
Source: rs215979566
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18676498G>A

Allele/Variant
Source: rs108108023
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18676561T>C

Allele/Variant
Source: rs245760046
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18676937G>A

Allele/Variant
Source: rs583440199
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18681284C>T

Allele/Variant
Source: rs587095199
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18681375C>G

Allele/Variant
Source: rs231342379
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18678934C>A

Allele/Variant
Source: rs216754678
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18696543T>C

Allele/Variant
Source: rs584476602
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18697749G>A

Allele/Variant
Source: rs108262052
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18701751C>T

Allele/Variant
Source: rs253328310
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18706182A>G

Allele/Variant
Source: rs251047336
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18706481C>T

Allele/Variant
Source: rs217634800
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18699177A>G

Allele/Variant
Source: rs239591304
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18704210A>G

Allele/Variant
Source: rs233065485
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18704386A>G

Allele/Variant
Source: rs219713824
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18706976C>T

Allele/Variant
Source: rs32380803
Genes: Hira (Mmu), Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18716205A>G

Allele/Variant
Source: rs579845742
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18658616G>A

Allele/Variant
Source: rs580200918
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18665531C>T

Allele/Variant
Source: rs584036952
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18665552G>A

Allele/Variant
Source: rs222954941
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18667856G>T

Allele/Variant
Source: rs257897452
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18674637C>T

Allele/Variant
Source: rs108083235
Genes: Gm28539 (Mmu), Mrpl40 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18690971C>T

Allele/Variant
Source: rs243526045
Genes: Gm28539 (Mmu), Mrpl40 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18694559A>G

Allele/Variant
Source: rs240261114
Genes: Gm28539 (Mmu), Mrpl40 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18694790A>T

Allele/Variant
Source: rs244238543
Genes: Gm28539 (Mmu), 2510002D24Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18655632T>A

Allele/Variant
Source: rs245994891
Genes: Gm28539 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)16:18660450A>G