Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SLC7A5 (Hsa)
(GRCh38)16:87832961G>C
(Homo sapiens)Allele/Variant
Source: rs141073967
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87832961G>C
(GRCh38)16:87832995A>T
(Homo sapiens)Allele/Variant
Source: rs2054951814
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87832995A>T
(GRCh38)16:87834422T>C
(Homo sapiens)Allele/Variant
Source: rs879766630
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834422T>C
(GRCh38)16:87869272T>C
(Homo sapiens)Allele/Variant
Source: rs760337387
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869272T>C
(GRCh38)16:87868964G>A
(Homo sapiens)Allele/Variant
Source: rs774535808
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87868964G>A
(GRCh38)16:87869347T>A
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87869347T>A
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869347T>A
(GRCh38)16:87832984G>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87832984G>T
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87832984G>T
(GRCh38)16:87836522C>A
(Homo sapiens)Allele/Variant
Source: rs769384114
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87836522C>A
(GRCh38)16:87836644C>G
(Homo sapiens)Allele/Variant
Source: rs777326719
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87836644C>G
(GRCh38)16:87837854G>A
(Homo sapiens)Allele/Variant
Source: rs2230174
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87837854G>A
(GRCh38)16:87834419C>A
(Homo sapiens)Allele/Variant
Source: rs564461426
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834419C>A
(GRCh38)16:87841083G>A
(Homo sapiens)Allele/Variant
Source: rs2143738378
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87841083G>A
(GRCh38)16:87869301C>T
(Homo sapiens)Allele/Variant
Source: rs148183733
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869301C>T
(GRCh38)16:87869329C>A
(Homo sapiens)Allele/Variant
Source: rs759266297
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869329C>A
(GRCh38)16:87851776C>A
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87851776C>A
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87851776C>A
(GRCh38)16:87834579G>C
(Homo sapiens)Allele/Variant
Source: rs1038464020
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834579G>C
(GRCh38)16:87834535G>C
(Homo sapiens)Allele/Variant
Source: rs11541881
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834535G>C
(GRCh38)16:87840438T>C
(Homo sapiens)Allele/Variant
Source: rs750247543
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87840438T>C
(GRCh38)16:87834540C>T
(Homo sapiens)Allele/Variant
Source: rs747038000
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834540C>T
(GRCh38)16:87868896C>A
(Homo sapiens)Allele/Variant
Source: rs1446589926
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87868896C>A
(GRCh38)16:87834456C>A
(Homo sapiens)Allele/Variant
Source: rs146583737
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834456C>A
(GRCh38)16:87869036G>A
(Homo sapiens)Allele/Variant
Source: rs33913122
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869036G>A
(GRCh38)16:87869078G>T
(Homo sapiens)Allele/Variant
Source: rs17853938
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869078G>T
(GRCh38)16:87836548C>T
(Homo sapiens)Allele/Variant
Source: rs777097653
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87836548C>T
(GRCh38)16:87838793C>T
(Homo sapiens)Allele/Variant
Source: rs771638454
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87838793C>T
(GRCh38)16:87839721G>A
(Homo sapiens)Allele/Variant
Source: rs202090522
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87839721G>A
(GRCh38)16:87841130G>C
(Homo sapiens)Allele/Variant
Source: rs1060250
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87841130G>C
(GRCh38)16:87868929G>A
(Homo sapiens)Allele/Variant
Source: rs771592683
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87868929G>A
(GRCh38)16:87869291C>G
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87869291C>G
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869291C>G
(GRCh38)16:87869392G>C
(Homo sapiens)Allele/Variant
Source: rs1299676066
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869392G>C
(GRCh38)16:87834417T>C
(Homo sapiens)Allele/Variant
Source: rs759073537
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834417T>C
(GRCh38)16:87836492G>T
(Homo sapiens)Allele/Variant
Source: rs371378644
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87836492G>T
(GRCh38)16:87838749G>A
(Homo sapiens)Allele/Variant
Source: rs1060251
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87838749G>A
(GRCh38)16:87841152T>A
(Homo sapiens)Allele/Variant
Source: rs17853937
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87841152T>A
(GRCh38)16:87869080C>T
(Homo sapiens)Allele/Variant
Source: rs2055499060
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869080C>T
(GRCh38)16:87869377C>T
(Homo sapiens)Allele/Variant
Source: rs1191984510
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869377C>T
(GRCh38)16:87869406G>A
(Homo sapiens)Allele/Variant
Source: rs33983951
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869406G>A
(GRCh38)16:87834582C>T
(Homo sapiens)Allele/Variant
Source: rs1157166399
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87834582C>T
(GRCh38)16:87869001C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87869001C>T
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869001C>T
(GRCh38)16:87836651G>T
(Homo sapiens)Allele/Variant
Source: rs986514243
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87836651G>T
(GRCh38)16:87837861G>A
(Homo sapiens)Allele/Variant
Source: rs757972971
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87837861G>A
(GRCh38)16:87838708G>A
(Homo sapiens)Allele/Variant
Source: rs33966404
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87838708G>A
(GRCh38)16:87838767G>A
(Homo sapiens)Allele/Variant
Source: rs777967482
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87838767G>A
(GRCh38)16:87851781C>T
(Homo sapiens)Allele/Variant
Source: rs151257488
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87851781C>T
(GRCh38)16:87851791G>A
(Homo sapiens)Allele/Variant
Source: rs33938662
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87851791G>A
(GRCh38)16:87851836G>C
(Homo sapiens)Allele/Variant
Source: rs549051612
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87851836G>C
(GRCh38)16:87869355C>G
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.87869355C>G
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869355C>G
(GRCh38)16:87869423G>A
(Homo sapiens)Allele/Variant
Source: rs779157899
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87869423G>A
(GRCh38)16:87839704C>T
(Homo sapiens)Allele/Variant
Source: rs780213182
Genes: SLC7A5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:87839704C>T