Version: 8.0.0
Date: Tue Jan 28 2025
5 results
Allele/Variant Genes: TMEFF1 (Hsa)

(GRCh38)9:100473724G>C

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.100473724G>C
Genes: MSANTD3-TMEFF1 (Hsa), TMEFF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:100473724G>C

(GRCh38)9:100473671C>T

(Homo sapiens)
Allele/Variant
Source: rs760451724
Genes: MSANTD3-TMEFF1 (Hsa), TMEFF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:100473671C>T

(GRCh38)9:100473555C>T

(Homo sapiens)
Allele/Variant
Source: rs767265770
Genes: MSANTD3-TMEFF1 (Hsa), TMEFF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:100473555C>T

(GRCh38)9:100473630T>A

(Homo sapiens)
Allele/Variant
Source: rs762424812
Genes: MSANTD3-TMEFF1 (Hsa), TMEFF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:100473630T>A

(GRCh38)9:100473554G>A

(Homo sapiens)
Allele/Variant
Source: rs754830275
Genes: MSANTD3-TMEFF1 (Hsa), TMEFF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:100473554G>A