48 results
Allele/Variant Genes: Wbp2 (Mmu) Molecular Consequence: non coding transcript exon variant
Allele/Variant
Source: rs259515002
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974249G>A

Allele/Variant
Source: rs223158127
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974269A>G

Allele/Variant
Source: rs263673621
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115970357A>G

Allele/Variant
Source: rs229123227
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972208G>A

Allele/Variant
Source: rs247481366
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972825G>A

Allele/Variant
Source: rs252553356
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974382A>G

Allele/Variant
Source: rs246626803
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115973145A>G

Allele/Variant
Source: rs248911353
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974541C>A

Allele/Variant
Source: rs225527284
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972235G>A

Allele/Variant
Source: rs263988096
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972207C>T

Allele/Variant
Source: rs219466546
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974084G>C

Allele/Variant
Source: rs251224352
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972274G>A

Allele/Variant
Source: rs243439444
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974280C>G

Allele/Variant
Source: rs1131848768
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974120T>C

Allele/Variant
Source: rs585210346
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974156C>A

Allele/Variant
Source: rs239651976
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974495G>A

Allele/Variant
Source: rs250378139
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115973972C>T

Allele/Variant
Source: rs29441479
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974097G>A

Allele/Variant
Source: rs212163551
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974606G>T

Allele/Variant
Source: rs1132921469
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115977741T>C

Allele/Variant
Source: rs231497650
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974321C>T

Allele/Variant
Source: rs224613672
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115970352C>T

Allele/Variant
Source: rs45748624
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974255C>T

Allele/Variant
Source: rs584546252
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972976T>C

Allele/Variant
Source: rs217420478
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974446A>T

Allele/Variant
Source: rs1132611964
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115973931G>C

Allele/Variant
Source: rs237109580
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972919A>C

Allele/Variant
Source: rs29405653
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972985G>A

Allele/Variant
Source: rs256644301
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972944C>T

Allele/Variant
Source: rs248027097
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974671C>T

Allele/Variant
Source: rs29486235
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115977764T>C

Allele/Variant
Source: rs225322413
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972805G>A

Allele/Variant
Source: rs580672154
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115971169C>T

Allele/Variant
Source: rs256607405
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972224G>A

Allele/Variant
Source: rs13459340
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115973135A>G

Allele/Variant
Source: rs265456424
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974112C>T

Allele/Variant
Source: rs48238135
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974252T>G

Allele/Variant
Source: rs232270497
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972656C>T

Allele/Variant
Source: rs1132367789
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974147G>T

Allele/Variant
Source: rs249789664
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974187C>T

Allele/Variant
Source: rs1134238089
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115977802G>A

Allele/Variant
Source: rs263735638
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972865G>A

Allele/Variant
Source: rs237021062
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972222T>G

Allele/Variant
Source: rs258786658
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972804G>T

Allele/Variant
Source: rs248949699
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972175G>A

Allele/Variant
Source: rs255765754
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974296C>A

Allele/Variant
Source: rs224753342
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115974177C>A

Allele/Variant
Source: rs223440857
Genes: Wbp2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:115972879G>A