Version: 8.0.0
Date: Tue Jan 28 2025
54 results
Allele/Variant Genes: let-60 (Cel)

s1155

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00241957
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

n2031

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090340
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

tm6614

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar02125207
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

s2336

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00242269
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

n1041

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00089914
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

sy101sy127

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar02125747
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

n1046

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00089919
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: RASopathy, cancer
Variant Name: Not Available

(WBcel235)IV:11690905C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690905C>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690905C>T

(WBcel235)IV:11688766G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688766G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688766G>A

(WBcel235)IV:11689619T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689619T>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689619T>A

(WBcel235)IV:11690607C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690607C>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690607C>T

(WBcel235)IV:11690733A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690733A>C
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690733A>C

(WBcel235)IV:11688569A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688569A>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688569A>T

(WBcel235)IV:11690349A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690349A>G
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690349A>G

(WBcel235)IV:11688389A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688389A>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688389A>T

(WBcel235)IV:11689585C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689585C>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689585C>T

(WBcel235)IV:11689945G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689945G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689945G>A

sy93

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248905
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy95

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248907
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy94

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248906
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

n2035

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090343
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

n1531

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090203
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

(WBcel235)IV:11688649G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688649G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688649G>A

(WBcel235)IV:11689030A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689030A>G
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689030A>G

(WBcel235)IV:11690952C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690952C>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690952C>T

(WBcel235)IV:11690475T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690475T>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690475T>A

(WBcel235)IV:11690927G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690927G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690927G>A

n2021

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090336
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

ga89

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00145416
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

s1124

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00241944
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy99

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248910
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy127

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248917
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

sy130

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248919
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

(WBcel235)IV:11688573G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688573G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688573G>A

(WBcel235)IV:11689895G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689895G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689895G>A

(WBcel235)IV:11690903T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690903T>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690903T>A

(WBcel235)IV:11690443G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690443G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690443G>A

(WBcel235)IV:11688263G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11688263G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11688263G>A

sy101

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248912
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy100

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248911
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy103

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248914
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy92

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248904
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

n1876

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090284
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

(WBcel235)IV:11689612C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11689612C>T
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11689612C>T

(WBcel235)IV:11690285G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690285G>A
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690285G>A

(WBcel235)IV:11690904G>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.11690904G>C
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:11690904G>C

s59

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00241691
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

sy163

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00248923
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

dx16

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00142881
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: 5_prime_UTR_variant, coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available

n1700

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00090238
Genes: let-60 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available