Version: 8.0.0
Date: Tue Jan 28 2025
2 results
Allele/Variant Genes: TXNDC9 (Hsa) Molecular Consequence: non coding transcript variant

(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