Version: 8.0.0
Date: Tue Jan 28 2025
4,998 results for tspan18

(GRCh38)11:44926684C>T

(Homo sapiens)
Allele/Variant
Source: rs781065961
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44926684C>T

(GRCh38)11:44909869C>T

(Homo sapiens)
Allele/Variant
Source: rs1217918419
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909869C>T

(GRCh38)11:44919960G>A

(Homo sapiens)
Allele/Variant
Source: rs267602882
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919960G>A

(GRCh38)11:44909757C>T

(Homo sapiens)
Allele/Variant
Source: rs34282417
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909757C>T

(GRCh38)11:44909758C>T

(Homo sapiens)
Allele/Variant
Source: rs755992011
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909758C>T

(GRCh38)11:44919967C>T

(Homo sapiens)
Allele/Variant
Source: rs1250058016
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919967C>T

(GRCh38)11:44918041G>A

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.44918041G>A
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44918041G>A

(GRCh38)11:44919844G>A

(Homo sapiens)
Allele/Variant
Source: rs760465322
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919844G>A

(GRCh38)11:44917975T>G

(Homo sapiens)
Allele/Variant
Source: rs376320762
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44917975T>G

(GRCh38)11:44919322G>A

(Homo sapiens)
Allele/Variant
Source: rs11038214
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919322G>A

(GRCh38)11:44909828G>T

(Homo sapiens)
Allele/Variant
Source: rs747575703
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909828G>T

(GRCh38)11:44906430G>A

(Homo sapiens)
Allele/Variant
Source: rs1471049309
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44906430G>A

(GRCh38)11:44909759G>A

(Homo sapiens)
Allele/Variant
Source: rs777649688
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909759G>A

(GRCh38)11:44909774G>A

(Homo sapiens)
Allele/Variant
Source: rs138512957
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909774G>A

(GRCh38)11:44909745T>C

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.44909745T>C
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909745T>C

(GRCh38)11:44926712C>T

(Homo sapiens)
Allele/Variant
Source: rs34695714
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44926712C>T

(GRCh38)11:44919277G>A

(Homo sapiens)
Allele/Variant
Source: rs2291334
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919277G>A

(GRCh38)11:44919940G>A

(Homo sapiens)
Allele/Variant
Source: rs759610514
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919940G>A

(GRCh38)11:44919955C>T

(Homo sapiens)
Allele/Variant
Source: rs752986300
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919955C>T

(GRCh38)11:44909873C>T

(Homo sapiens)
Allele/Variant
Source: rs771284701
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44909873C>T

(GRCh38)11:44917989G>T

(Homo sapiens)
Allele/Variant
Source: rs142957647
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44917989G>T

(GRCh38)11:44919969C>T

(Homo sapiens)
Allele/Variant
Source: rs200276331
Genes: TSPAN18 (Hsa), TP53I11 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:44919969C>T

(mRatBN7.2)3:79163145G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197193342
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79163145G>T

(mRatBN7.2)3:79229578A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105418240
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79229578A>G

(mRatBN7.2)3:79230347G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319959896
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79230347G>T

(mRatBN7.2)3:79215639G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319894734
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79215639G>A

(mRatBN7.2)3:79216687A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319959958
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79216687A>G

(mRatBN7.2)3:79225833G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.79225833G>C
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79225833G>C

(mRatBN7.2)3:79225894G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319942157
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79225894G>T

(mRatBN7.2)3:79233006T>C

(Rattus norvegicus)
Allele/Variant
Source: rs65455602
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79233006T>C

(mRatBN7.2)3:79167667A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105979322
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79167667A>C

(mRatBN7.2)3:79176413C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197308203
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79176413C>T

(mRatBN7.2)3:79174284A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199175841
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79174284A>G

(mRatBN7.2)3:79177153G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198830944
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79177153G>A

(mRatBN7.2)3:79182046C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105363288
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79182046C>G

(mRatBN7.2)3:79219367G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197282972
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79219367G>A

(mRatBN7.2)3:79220579A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.79220579A>G
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79220579A>G

(mRatBN7.2)3:79220647C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.79220647C>T
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79220647C>T

(mRatBN7.2)3:79269618T>A

(Rattus norvegicus)
Allele/Variant
Source: rs107244365
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79269618T>A

(mRatBN7.2)3:79270611C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197800130
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79270611C>T

(mRatBN7.2)3:79274325A>T

(Rattus norvegicus)
Allele/Variant
Source: rs197438828
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79274325A>T

(mRatBN7.2)3:79259943G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105775248
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79259943G>A

(mRatBN7.2)3:79165308T>C

(Rattus norvegicus)
Allele/Variant
Source: rs63795216
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79165308T>C

(mRatBN7.2)3:79166807T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198757537
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79166807T>C

(mRatBN7.2)3:79170873G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106923756
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79170873G>A

(mRatBN7.2)3:79174295G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319942129
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79174295G>A

(mRatBN7.2)3:79180855T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319941513
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79180855T>A

(mRatBN7.2)3:79194034C>G

(Rattus norvegicus)
Allele/Variant
Source: rs107154518
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79194034C>G

(mRatBN7.2)3:79194104G>C

(Rattus norvegicus)
Allele/Variant
Source: rs106772429
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79194104G>C

(mRatBN7.2)3:79211052T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319940967
Genes: Tspan18 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:79211052T>C