Version: 8.0.0
Date: Tue Jan 28 2025
10 results
Allele/Variant Genes: TXNDC9 (Hsa)

(GRCh38)2:99319726T>G

(Homo sapiens)
Allele/Variant
Source: rs1213875510
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99319726T>G

(GRCh38)2:99321973G>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.99321973G>A
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99321973G>A

(GRCh38)2:99333074C>T

(Homo sapiens)
Allele/Variant
Source: rs767681836
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333074C>T

(GRCh38)2:99322130T>C

(Homo sapiens)
Allele/Variant
Source: rs750758972
Genes: TXNDC9 (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)2:99322130T>C

(GRCh38)2:99333075G>A

(Homo sapiens)
Allele/Variant
Source: rs866880642
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333075G>A

(GRCh38)2:99322028G>C

(Homo sapiens)
Allele/Variant
Source: rs761714942
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99322028G>C

(GRCh38)2:99337578G>C

(Homo sapiens)
Allele/Variant
Source: rs752474657
Genes: TXNDC9 (Hsa), EIF5B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99337578G>C

(GRCh38)2:99327537G>C

(Homo sapiens)
Allele/Variant
Source: rs1217226709
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99327537G>C

(GRCh38)2:99322164G>T

(Homo sapiens)
Allele/Variant
Source: rs908232770
Genes: TXNDC9 (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)2:99322164G>T

(GRCh38)2:99333044C>T

(Homo sapiens)
Allele/Variant
Source: rs1403241808
Genes: TXNDC9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:99333044C>T