2,124 results
Allele/Variant Genes: Abl2 (Mmu)

Abl2Gt(kin)Byg

(Mus musculus)
Allele/Variant
Source: MGI:4458329
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2tm1c(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:6111513
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2tm2.1Ajk

(Mus musculus)
Allele/Variant
Source: MGI:6369395
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2tm1Ajk

(Mus musculus)
Allele/Variant
Source: MGI:2153719
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2Gt(OST407367)Lex

(Mus musculus)
Allele/Variant
Source: MGI:3530057
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2tm1a(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5444979
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Abl2em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:6367962
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs221231528
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386211C>T

Allele/Variant
Source: rs243606773
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156387042A>G

Allele/Variant
Source: rs30643677
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156387761G>A

Allele/Variant
Source: rs31276160
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156402817C>G

Allele/Variant
Source: rs247755926
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156403181T>C

Allele/Variant
Source: rs259121961
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156390206G>A

Allele/Variant
Source: rs578654945
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156389994G>A

Allele/Variant
Source: rs217715365
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156397310G>A

Allele/Variant
Source: rs247517936
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156398532C>T

Allele/Variant
Source: rs231234912
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156390882T>A

Allele/Variant
Source: rs583510599
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386278T>C

Allele/Variant
Source: rs225939117
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156387475T>C

Allele/Variant
Source: rs587254052
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156402641G>A

Allele/Variant
Source: rs258145831
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156394763C>T

Allele/Variant
Source: rs252995263
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156397825C>T

Allele/Variant
Source: rs256129515
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156404001G>A

Allele/Variant
Source: rs238013484
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156404585A>T

Allele/Variant
Source: rs215822178
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156392760A>G

Allele/Variant
Source: rs1134040223
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156404856A>C

Allele/Variant
Source: rs50143915
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156412557G>A

Allele/Variant
Source: rs219295813
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386179G>A

Allele/Variant
Source: rs250787247
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156417248A>G

Allele/Variant
Source: rs48422200
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156413066G>A

Allele/Variant
Source: rs247531294
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156413322A>G

Allele/Variant
Source: rs52225925
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156434868G>A

Allele/Variant
Source: rs254494994
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156430996G>T

Allele/Variant
Source: rs31275125
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156406506C>A

Allele/Variant
Source: rs52259675
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156434905T>C

Allele/Variant
Source: rs242857238
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156437475T>G

Allele/Variant
Source: rs215816652
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156437580T>A

Allele/Variant
Source: rs586843524
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386283C>G

Allele/Variant
Source: rs253867108
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386189A>C

Allele/Variant
Source: rs49122249
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156386609G>A

Allele/Variant
Source: rs227923873
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156391609G>A

Allele/Variant
Source: rs212593442
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156407853G>A

Allele/Variant
Source: rs213611719
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156390467G>C

Allele/Variant
Source: rs245626784
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156392576T>C

Allele/Variant
Source: rs256746582
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156392578A>C

Allele/Variant
Source: rs242273445
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156404148C>T

Allele/Variant
Source: rs30688466
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156393379A>G

Allele/Variant
Source: rs50355478
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156412594C>T

Allele/Variant
Source: rs578287464
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156403897A>G

Allele/Variant
Source: rs234322564
Genes: Abl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:156398743A>G