Version: 8.0.0
Date: Tue Jan 28 2025

Allele/Variant

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24 results
Allele/Variant Genes: GLTPD2 (Hsa)

(GRCh38)17:4789958T>C

(Homo sapiens)
Allele/Variant
Source: rs199986886
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789958T>C

(GRCh38)17:4790018G>A

(Homo sapiens)
Allele/Variant
Source: NC_000017.11:g.4790018G>A
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790018G>A

(GRCh38)17:4790271A>G

(Homo sapiens)
Allele/Variant
Source: rs765238837
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790271A>G

(GRCh38)17:4789084C>G

(Homo sapiens)
Allele/Variant
Source: NC_000017.11:g.4789084C>G
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789084C>G

(GRCh38)17:4789582G>A

(Homo sapiens)
Allele/Variant
Source: rs375244706
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789582G>A

(GRCh38)17:4789831G>T

(Homo sapiens)
Allele/Variant
Source: rs374100494
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789831G>T

(GRCh38)17:4789581T>G

(Homo sapiens)
Allele/Variant
Source: rs954565904
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789581T>G

(GRCh38)17:4789788C>T

(Homo sapiens)
Allele/Variant
Source: rs1567712319
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789788C>T

(GRCh38)17:4789929C>T

(Homo sapiens)
Allele/Variant
Source: rs750635969
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789929C>T

(GRCh38)17:4789961C>T

(Homo sapiens)
Allele/Variant
Source: NC_000017.11:g.4789961C>T
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789961C>T

(GRCh38)17:4790015C>G

(Homo sapiens)
Allele/Variant
Source: rs971374901
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790015C>G

(GRCh38)17:4790072T>A

(Homo sapiens)
Allele/Variant
Source: rs973091317
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790072T>A

(GRCh38)17:4789028G>A

(Homo sapiens)
Allele/Variant
Source: rs200715683
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789028G>A

(GRCh38)17:4790150C>T

(Homo sapiens)
Allele/Variant
Source: rs369571991
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790150C>T

(GRCh38)17:4790273C>G

(Homo sapiens)
Allele/Variant
Source: rs1350396870
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790273C>G

(GRCh38)17:4789899G>A

(Homo sapiens)
Allele/Variant
Source: rs973259137
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789899G>A

(GRCh38)17:4790088G>C

(Homo sapiens)
Allele/Variant
Source: rs1316615097
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790088G>C

(GRCh38)17:4790189G>C

(Homo sapiens)
Allele/Variant
Source: rs1375502403
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790189G>C

(GRCh38)17:4789253C>T

(Homo sapiens)
Allele/Variant
Source: rs373630469
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789253C>T

(GRCh38)17:4789273G>C

(Homo sapiens)
Allele/Variant
Source: rs202226463
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789273G>C

(GRCh38)17:4789926C>T

(Homo sapiens)
Allele/Variant
Source: rs373390253
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789926C>T

(GRCh38)17:4789980A>G

(Homo sapiens)
Allele/Variant
Source: rs1567712496
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4789980A>G

(GRCh38)17:4790062C>G

(Homo sapiens)
Allele/Variant
Source: NC_000017.11:g.4790062C>G
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790062C>G

(GRCh38)17:4790079C>A

(Homo sapiens)
Allele/Variant
Source: rs1184165883
Genes: GLTPD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:4790079C>A