Version: 8.0.0
Date: Tue Jan 28 2025
10 results
Allele/Variant Genes: TRAF3IP3 (Hsa) Molecular Consequence: 3 prime UTR variant

(GRCh38)1:209780484G>A

(Homo sapiens)
Allele/Variant
Source: rs758375285
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780484G>A

(GRCh38)1:209782089G>A

(Homo sapiens)
Allele/Variant
Source: rs141902362
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209782089G>A

(GRCh38)1:209780592G>A

(Homo sapiens)
Allele/Variant
Source: rs1032979701
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780592G>A

(GRCh38)1:209781403G>A

(Homo sapiens)
Allele/Variant
Source: rs771216589
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781403G>A

(GRCh38)1:209775703G>C

(Homo sapiens)
Allele/Variant
Source: rs377426065
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209775703G>C

(GRCh38)1:209775600G>A

(Homo sapiens)
Allele/Variant
Source: rs200380274
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209775600G>A

(GRCh38)1:209781421G>A

(Homo sapiens)
Allele/Variant
Source: rs544408933
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781421G>A

(GRCh38)1:209781373A>G

(Homo sapiens)
Allele/Variant
Source: rs1306183518
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209781373A>G

(GRCh38)1:209777484C>A

(Homo sapiens)
Allele/Variant
Source: rs1031910707
Genes: TRAF3IP3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209777484C>A

(GRCh38)1:209780527G>A

(Homo sapiens)
Allele/Variant
Source: rs1180866483
Genes: TRAF3IP3 (Hsa), C1orf74 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:209780527G>A