165 results for TGFB2-AS1

TGFB2-AS1

(Homo sapiens)
Gene
Name: TGFB2 antisense RNA 1 (head to head)
Synonyms: Not Available
Source: HGNC:50628
Biotype: ncRNA gene
Symbol: TGFB2-AS1 (Hsa)
Symbol: TGFB2-AS1

Allele/Variant
Source: rs7550232
Genes: TGFB2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218345173A>C

Allele/Variant
Source: rs1571820524
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346698A>C

Allele/Variant
Source: rs776628524
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346712G>A

Allele/Variant
Source: rs765477784
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346721G>C

Allele/Variant
Source: rs1656693157
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346739A>G

Allele/Variant
Source: rs886045975
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346753G>T

Allele/Variant
Source: rs781126315
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346755G>T

Allele/Variant
Source: NC_000001.11:g.218346774A>C
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346774A>C

Allele/Variant
Source: rs1571820734
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346801C>T

Allele/Variant
Source: rs1064796462
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346802G>A

Allele/Variant
Source: NC_000001.11:g.218346732A>C
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346732A>C

Allele/Variant
Source: rs763918203
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346738C>A

Allele/Variant
Source: rs1224916923
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346758C>T

Allele/Variant
Source: rs1656695125
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346760G>C

Allele/Variant
Source: NC_000001.11:g.218346779A>G
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346779A>G

Allele/Variant
Source: rs1656697535
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346813G>C

Allele/Variant
Source: rs149215818
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346815G>A

Allele/Variant
Source: NC_000001.11:g.218346822C>T
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346822C>T

Allele/Variant
Source: NC_000001.11:g.218346828C>T
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346828C>T

Allele/Variant
Source: rs2102527511
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346843C>T

Allele/Variant
Source: rs1656685944
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346601A>G

Allele/Variant
Source: rs1656695125
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346760G>A

Allele/Variant
Source: NC_000001.11:g.218346782C>A
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346782C>A

Allele/Variant
Source: rs10482720
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346807A>C

Allele/Variant
Source: rs1558220033
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346826G>A

Allele/Variant
Source: rs1318854254
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346838G>A

Allele/Variant
Source: rs1553292088
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346844T>G

Allele/Variant
Source: rs73110310
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218345988A>C

Allele/Variant
Source: rs886045961
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346003A>C

Allele/Variant
Source: rs1018085683
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346086G>A

Allele/Variant
Source: rs1004111898
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346606C>A

Allele/Variant
Source: rs886045975
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346753G>A

Allele/Variant
Source: NC_000001.11:g.218346785T>C
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346785T>C

Allele/Variant
Source: rs2102527486
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346820T>A

Allele/Variant
Source: rs769913843
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346863A>G

Allele/Variant
Source: rs750324465
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346895C>T

Allele/Variant
Source: rs1656702743
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346909A>G

Allele/Variant
Source: rs1027195424
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346910T>C

Allele/Variant
Source: rs886042712
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218347052G>A

Allele/Variant
Source: rs1557153
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218345918A>C

Allele/Variant
Source: rs2102527478
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346817C>T

Allele/Variant
Source: rs897070997
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346872T>A

Allele/Variant
Source: rs747128130
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346894C>T

Allele/Variant
Source: rs201761868
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346900G>A

Allele/Variant
Source: rs766024374
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218346914C>A

Allele/Variant
Source: rs753391734
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346918A>G

Allele/Variant
Source: rs781392453
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346952G>A

Allele/Variant
Source: rs2102527749
Genes: TGFB2-AS1 (Hsa), TGFB2 (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)1:218346955G>A

Allele/Variant
Source: rs1656628678
Genes: TGFB2-AS1 (Hsa), TGFB2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:218345465G>C