Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TRPV2 (Hsa)
(GRCh38)17:16428933A>G
(Homo sapiens)Allele/Variant
Source: rs768382920
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16428933A>G
(GRCh38)17:16436866G>A
(Homo sapiens)Allele/Variant
Source: rs150619451
Genes: TRPV2 (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)17:16436866G>A
(GRCh38)17:16433681T>A
(Homo sapiens)Allele/Variant
Source: rs1326280728
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16433681T>A
(GRCh38)17:16426220G>A
(Homo sapiens)Allele/Variant
Source: rs201401044
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16426220G>A
(GRCh38)17:16427514C>G
(Homo sapiens)Allele/Variant
Source: rs201825898
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16427514C>G
(GRCh38)17:16428935A>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.16428935A>G
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16428935A>G
(GRCh38)17:16432169G>A
(Homo sapiens)Allele/Variant
Source: rs772205239
Genes: TRPV2 (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)17:16432169G>A
(GRCh38)17:16423711C>T
(Homo sapiens)Allele/Variant
Source: rs373078008
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423711C>T
(GRCh38)17:16427539G>A
(Homo sapiens)Allele/Variant
Source: rs372298752
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16427539G>A
(GRCh38)17:16417816T>C
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.16417816T>C
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16417816T>C
(GRCh38)17:16420132G>A
(Homo sapiens)Allele/Variant
Source: rs569542610
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16420132G>A
(GRCh38)17:16423592A>G
(Homo sapiens)Allele/Variant
Source: rs747027326
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423592A>G
(GRCh38)17:16417811G>A
(Homo sapiens)Allele/Variant
Source: rs375026490
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16417811G>A
(GRCh38)17:16420162T>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.16420162T>G
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16420162T>G
(GRCh38)17:16423658G>A
(Homo sapiens)Allele/Variant
Source: rs267604756
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)17:16423658G>A
(GRCh38)17:16433617G>A
(Homo sapiens)Allele/Variant
Source: rs770721097
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16433617G>A
(GRCh38)17:16420120C>T
(Homo sapiens)Allele/Variant
Source: rs549676530
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16420120C>T
(GRCh38)17:16427485T>C
(Homo sapiens)Allele/Variant
Source: rs1355028326
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16427485T>C
(GRCh38)17:16432161A>G
(Homo sapiens)Allele/Variant
Source: rs112697098
Genes: TRPV2 (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)17:16432161A>G
(GRCh38)17:16436850G>T
(Homo sapiens)Allele/Variant
Source: rs374417810
Genes: TRPV2 (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)17:16436850G>T
(GRCh38)17:16432085G>A
(Homo sapiens)Allele/Variant
Source: rs201685191
Genes: TRPV2 (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)17:16432085G>A
(GRCh38)17:16417810C>T
(Homo sapiens)Allele/Variant
Source: rs368136795
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16417810C>T
(GRCh38)17:16428313G>A
(Homo sapiens)Allele/Variant
Source: rs201142576
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16428313G>A
(GRCh38)17:16432045G>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.16432045G>A
Genes: TRPV2 (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)17:16432045G>A
(GRCh38)17:16420168G>A
(Homo sapiens)Allele/Variant
Source: rs144086701
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16420168G>A
(GRCh38)17:16423549G>A
(Homo sapiens)Allele/Variant
Source: rs143117492
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423549G>A
(GRCh38)17:16427475G>C
(Homo sapiens)Allele/Variant
Source: rs748553622
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16427475G>C
(GRCh38)17:16423549G>T
(Homo sapiens)Allele/Variant
Source: rs143117492
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423549G>T
(GRCh38)17:16422688G>C
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.16422688G>C
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16422688G>C
(GRCh38)17:16422769A>G
(Homo sapiens)Allele/Variant
Source: rs139207152
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16422769A>G
(GRCh38)17:16423732C>A
(Homo sapiens)Allele/Variant
Source: rs755105135
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423732C>A
(GRCh38)17:16417855G>A
(Homo sapiens)Allele/Variant
Source: rs774399040
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16417855G>A
(GRCh38)17:16423765G>A
(Homo sapiens)Allele/Variant
Source: rs200335082
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16423765G>A
(GRCh38)17:16431844G>A
(Homo sapiens)Allele/Variant
Source: rs754548112
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16431844G>A
(GRCh38)17:16427477T>C
(Homo sapiens)Allele/Variant
Source: rs1309255970
Genes: TRPV2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:16427477T>C