142 results
Allele/Variant Genes: Insl5 (Mmu)

Insl5tm1Dgen

(Mus musculus)
Allele/Variant
Source: MGI:3604599
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Insl5em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7300858
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Insl5em3Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7300859
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Insl5tm1Imad

(Mus musculus)
Allele/Variant
Source: MGI:5445709
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs28194187
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883240C>T

Allele/Variant
Source: rs28194204
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875509C>T

Allele/Variant
Source: rs28194175
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884001T>C

Allele/Variant
Source: rs28194199
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875912C>T

Allele/Variant
Source: rs257524620
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882903T>C

Allele/Variant
Source: rs230702619
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882950G>A

Allele/Variant
Source: rs231241520
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875223C>T

Allele/Variant
Source: rs262928629
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883247C>T

Allele/Variant
Source: rs259348436
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883292A>T

Allele/Variant
Source: rs582485944
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883544G>A

Allele/Variant
Source: rs238675576
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883690T>A

Allele/Variant
Source: rs28194180
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883779A>G

Allele/Variant
Source: rs256516272
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883897G>A

Allele/Variant
Source: rs249187201
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875737T>C

Allele/Variant
Source: rs237644355
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875932C>A

Allele/Variant
Source: rs28194174
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: start_lost
Diseases: Not Available
Variant Name: (GRCm39)4:102884039T>G

Allele/Variant
Source: rs28194173
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884203A>G

Allele/Variant
Source: rs28194172
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884243T>C

Allele/Variant
Source: rs255122138
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882586T>G

Allele/Variant
Source: rs224104579
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882587T>A

Allele/Variant
Source: rs28194191
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883118C>T

Allele/Variant
Source: rs232745189
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883168T>C

Allele/Variant
Source: rs581591977
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883311G>A

Allele/Variant
Source: rs28194182
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883746T>C

Allele/Variant
Source: rs28194179
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883803A>G

Allele/Variant
Source: rs262929972
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884210G>A

Allele/Variant
Source: rs28194211
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875216C>T

Allele/Variant
Source: rs253475073
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875241A>C

Allele/Variant
Source: rs1133251196
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102876446C>G

Allele/Variant
Source: rs28194197
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882688C>A

Allele/Variant
Source: rs256985862
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883071G>A

Allele/Variant
Source: rs241638907
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883143C>G

Allele/Variant
Source: rs28194188
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883209G>A

Allele/Variant
Source: rs28194186
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883266G>T

Allele/Variant
Source: rs243359313
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883274G>A

Allele/Variant
Source: rs28194185
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102883280C>T

Allele/Variant
Source: rs241890881
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875152T>C

Allele/Variant
Source: rs28194214
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875159A>G

Allele/Variant
Source: rs28194206
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875420T>A

Allele/Variant
Source: rs580830186
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875565C>G

Allele/Variant
Source: rs219929713
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884070G>A

Allele/Variant
Source: rs1132391818
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102884238G>T

Allele/Variant
Source: rs258008263
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102875935T>C

Allele/Variant
Source: rs32134486
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882098A>G

Allele/Variant
Source: rs249301942
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882467C>T

Allele/Variant
Source: rs218815520
Genes: Insl5 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:102882506T>C