66 results for T10B5.2

T10B5.2

(Caenorhabditis elegans)
Gene
Name: Not Available
Synonyms: CELE_T10B5.2
Source: WB:WBGene00020388
Biotype: pseudogene
Symbol: T10B5.2 (Cel)
Symbol: T10B5.2
Cross References: WB:T10B5.2...T10B5.2...T10B5.2

(WBcel235)V:1851254C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851254C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851254C>T
Gene Cross References: T10B5.2

(WBcel235)V:1848832A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848832A>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848832A>T
Gene Cross References: T10B5.2

(WBcel235)V:1849241C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849241C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849241C>T
Gene Cross References: T10B5.2

(WBcel235)V:1848268G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848268G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848268G>A
Gene Cross References: T10B5.2

(WBcel235)V:1848337C>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848337C>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848337C>A
Gene Cross References: T10B5.2

(WBcel235)V:1850999A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850999A>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850999A>T
Gene Cross References: T10B5.2

(WBcel235)V:1848507G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848507G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848507G>A
Gene Cross References: T10B5.2

(WBcel235)V:1850197T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850197T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850197T>C
Gene Cross References: T10B5.2

(WBcel235)V:1850610G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850610G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850610G>A
Gene Cross References: T10B5.2

(WBcel235)V:1851426G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851426G>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851426G>T
Gene Cross References: T10B5.2

(WBcel235)V:1849761C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849761C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849761C>T
Gene Cross References: T10B5.2

(WBcel235)V:1849660G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849660G>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849660G>T
Gene Cross References: T10B5.2

(WBcel235)V:1848562G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848562G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848562G>A
Gene Cross References: T10B5.2

(WBcel235)V:1851173G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851173G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851173G>A
Gene Cross References: T10B5.2

(WBcel235)V:1848149T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848149T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848149T>C
Gene Cross References: T10B5.2

(WBcel235)V:1850006A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850006A>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850006A>G
Gene Cross References: T10B5.2

(WBcel235)V:1850873C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850873C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850873C>T
Gene Cross References: T10B5.2

(WBcel235)V:1849794T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849794T>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849794T>A
Gene Cross References: T10B5.2

(WBcel235)V:1848711C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848711C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848711C>T
Gene Cross References: T10B5.2

(WBcel235)V:1848073C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848073C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848073C>T
Gene Cross References: T10B5.2

(WBcel235)V:1849721C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849721C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849721C>T
Gene Cross References: T10B5.2

(WBcel235)V:1849929G>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849929G>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849929G>T
Gene Cross References: T10B5.2

(WBcel235)V:1851366G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851366G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851366G>A
Gene Cross References: T10B5.2

(WBcel235)V:1850097C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850097C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850097C>T
Gene Cross References: T10B5.2

(WBcel235)V:1848075C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848075C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848075C>T
Gene Cross References: T10B5.2

(WBcel235)V:1851081T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851081T>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851081T>G
Gene Cross References: T10B5.2

(WBcel235)V:1848463T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848463T>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848463T>A
Gene Cross References: T10B5.2

(WBcel235)V:1850565T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850565T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850565T>C
Gene Cross References: T10B5.2

(WBcel235)V:1848650A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848650A>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848650A>G
Gene Cross References: T10B5.2

(WBcel235)V:1848674T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848674T>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848674T>A
Gene Cross References: T10B5.2

(WBcel235)V:1849083G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849083G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849083G>A
Gene Cross References: T10B5.2

(WBcel235)V:1849161T>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849161T>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849161T>G
Gene Cross References: T10B5.2

(WBcel235)V:1848795G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848795G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848795G>A
Gene Cross References: T10B5.2

(WBcel235)V:1850087C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850087C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850087C>T
Gene Cross References: T10B5.2

(WBcel235)V:1850491G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850491G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850491G>A
Gene Cross References: T10B5.2

(WBcel235)V:1849951G>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849951G>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849951G>C
Gene Cross References: T10B5.2

(WBcel235)V:1851222G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851222G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851222G>A
Gene Cross References: T10B5.2

(WBcel235)V:1851438T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851438T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851438T>C
Gene Cross References: T10B5.2

(WBcel235)V:1848629A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848629A>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848629A>G
Gene Cross References: T10B5.2

(WBcel235)V:1849490A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849490A>G
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849490A>G
Gene Cross References: T10B5.2

(WBcel235)V:1848106T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848106T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848106T>C
Gene Cross References: T10B5.2

(WBcel235)V:1848560G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848560G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848560G>A
Gene Cross References: T10B5.2

(WBcel235)V:1850598T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850598T>C
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850598T>C
Gene Cross References: T10B5.2

(WBcel235)V:1850985C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850985C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850985C>T
Gene Cross References: T10B5.2

(WBcel235)V:1851016C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1851016C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1851016C>T
Gene Cross References: T10B5.2

(WBcel235)V:1848905A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1848905A>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1848905A>T
Gene Cross References: T10B5.2

(WBcel235)V:1849774G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849774G>A
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849774G>A
Gene Cross References: T10B5.2

(WBcel235)V:1849850A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1849850A>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1849850A>T
Gene Cross References: T10B5.2

(WBcel235)V:1850821C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003283.11:g.1850821C>T
Genes: T10B5.2 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (WBcel235)V:1850821C>T
Gene Cross References: T10B5.2