Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant Molecular Consequence: non coding transcript exon variant
(GRCh38)4:153712556C>T
(Homo sapiens)Allele/Variant
Source: rs200984268
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712556C>T
(GRCh38)4:153748728T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153748728T>C
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153748728T>C
(GRCh38)4:153712575A>G
(Homo sapiens)Allele/Variant
Source: rs781620641
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712575A>G
(GRCh38)4:153720281T>C
(Homo sapiens)Allele/Variant
Source: rs766883578
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720281T>C
(GRCh38)4:153728211G>A
(Homo sapiens)Allele/Variant
Source: rs201556317
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153728211G>A
(GRCh38)4:153728307A>G
(Homo sapiens)Allele/Variant
Source: rs374840860
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153728307A>G
(GRCh38)4:153728211G>T
(Homo sapiens)Allele/Variant
Source: rs201556317
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153728211G>T
(GRCh38)4:153720197G>A
(Homo sapiens)Allele/Variant
Source: rs765834231
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720197G>A
(GRCh38)4:153720284A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153720284A>G
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720284A>G
(GRCh38)4:153723399C>T
(Homo sapiens)Allele/Variant
Source: rs764124998
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723399C>T
(GRCh38)4:153748763T>C
(Homo sapiens)Allele/Variant
Source: rs764889075
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153748763T>C
(GRCh38)4:153720219C>T
(Homo sapiens)Allele/Variant
Source: rs201891647
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153720219C>T
(GRCh38)4:153751442A>G
(Homo sapiens)Allele/Variant
Source: rs554858143
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153751442A>G
(GRCh38)4:153712533T>C
(Homo sapiens)Allele/Variant
Source: rs774478741
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712533T>C
(GRCh38)4:153715537A>C
(Homo sapiens)Allele/Variant
Source: rs142224306
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153715537A>C
(GRCh38)4:153712496A>G
(Homo sapiens)Allele/Variant
Source: rs528121328
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153712496A>G
(GRCh38)4:153723406C>T
(Homo sapiens)Allele/Variant
Source: rs1219355122
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723406C>T
(GRCh38)4:153728243C>G
(Homo sapiens)Allele/Variant
Source: rs754691648
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153728243C>G
(GRCh38)4:153723355A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.153723355A>G
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153723355A>G
(GRCh38)4:153728297C>T
(Homo sapiens)Allele/Variant
Source: rs746352762
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153728297C>T
(GRCh38)4:153748749G>A
(Homo sapiens)Allele/Variant
Source: rs200438202
Genes: RNF175 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:153748749G>A