328 results
Allele/Variant Genes: Sap30l (Mmu)

Sap30lem1Mbp

(Mus musculus)
Allele/Variant
Source: MGI:6857724
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs29477122
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57693696C>T

Allele/Variant
Source: rs235227053
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694028T>C

Allele/Variant
Source: rs223730002
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694259C>T

Allele/Variant
Source: rs29423873
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694730G>A

Allele/Variant
Source: rs242333051
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57692461C>T

Allele/Variant
Source: rs265130394
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57693259C>G

Allele/Variant
Source: rs229233771
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57693505G>A

Allele/Variant
Source: rs235802620
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694262C>A

Allele/Variant
Source: rs253987069
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694300G>A

Allele/Variant
Source: rs228397059
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695710T>G

Allele/Variant
Source: rs26980952
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694493A>C

Allele/Variant
Source: rs236812466
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694967G>T

Allele/Variant
Source: rs253382323
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695450C>G

Allele/Variant
Source: rs48197899
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695477A>G

Allele/Variant
Source: rs218781004
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695684T>C

Allele/Variant
Source: rs215419752
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695792G>A

Allele/Variant
Source: rs261403478
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57698631T>C

Allele/Variant
Source: rs241825212
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57698635A>T

Allele/Variant
Source: rs249963691
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699100G>A

Allele/Variant
Source: rs580620832
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57700282G>A

Allele/Variant
Source: rs580183687
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699315C>T

Allele/Variant
Source: rs50981468
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699329G>A

Allele/Variant
Source: rs245629024
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699515C>G

Allele/Variant
Source: rs26980941
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699892C>T

Allele/Variant
Source: rs52097310
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57700273T>C

Allele/Variant
Source: rs583224077
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57700914G>A

Allele/Variant
Source: rs243064900
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57700927G>A

Allele/Variant
Source: rs29467093
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57701450C>T

Allele/Variant
Source: rs265109594
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57701536A>G

Allele/Variant
Source: rs50572696
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57701761C>G

Allele/Variant
Source: rs29383769
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57694178A>G

Allele/Variant
Source: rs584461879
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695351G>C

Allele/Variant
Source: rs245567308
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57696390T>G

Allele/Variant
Source: rs224739230
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57696539C>G

Allele/Variant
Source: rs239560919
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57696616A>T

Allele/Variant
Source: rs250991476
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57697063T>C

Allele/Variant
Source: rs29438681
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57698287C>T

Allele/Variant
Source: rs29453855
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57698506C>G

Allele/Variant
Source: rs216544885
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699131G>A

Allele/Variant
Source: rs252437596
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57699375T>G

Allele/Variant
Source: rs26980944
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57697885G>A

Allele/Variant
Source: rs48766663
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57703354C>T

Allele/Variant
Source: rs243330240
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57703401A>G

Allele/Variant
Source: rs26980935
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57703430A>G

Allele/Variant
Source: rs26980934
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57703499C>T

Allele/Variant
Source: rs224053492
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57703612A>T

Allele/Variant
Source: rs52313050
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695328C>T

Allele/Variant
Source: rs244092804
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695434C>T

Allele/Variant
Source: rs240921327
Genes: Sap30l (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:57695712A>G