Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: LIFR (Hsa)
(GRCh38)5:38530504A>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38530504A>T
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38530504A>T
(GRCh38)5:38530552T>C
(Homo sapiens)Allele/Variant
Source: rs771905123
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38530552T>C
(GRCh38)5:38476791G>A
(Homo sapiens)Allele/Variant
Source: rs55917124
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38476791G>A
(GRCh38)5:38478146C>A
(Homo sapiens)Allele/Variant
Source: rs147793103
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38478146C>A
(GRCh38)5:38480590T>C
(Homo sapiens)Allele/Variant
Source: rs3776424
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38480590T>C
(GRCh38)5:38475495C>T
(Homo sapiens)Allele/Variant
Source: rs188682396
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38475495C>T
(GRCh38)5:38476535A>T
(Homo sapiens)Allele/Variant
Source: rs183333459
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38476535A>T
(GRCh38)5:38482686T>C
(Homo sapiens)Allele/Variant
Source: rs1744060535
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38482686T>C
(GRCh38)5:38493599A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38493599A>G
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38493599A>G
(GRCh38)5:38502780C>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38502780C>A
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38502780C>A
(GRCh38)5:38478125C>A
(Homo sapiens)Allele/Variant
Source: rs886467983
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38478125C>A
(GRCh38)5:38476370G>A
(Homo sapiens)Allele/Variant
Source: rs58755763
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38476370G>A
(GRCh38)5:38476411C>T
(Homo sapiens)Allele/Variant
Source: rs886060609
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38476411C>T
(GRCh38)5:38481829C>T
(Homo sapiens)Allele/Variant
Source: rs537706381
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38481829C>T
(GRCh38)5:38482002C>T
(Homo sapiens)Allele/Variant
Source: rs770022153
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38482002C>T
(GRCh38)5:38482685T>C
(Homo sapiens)Allele/Variant
Source: rs1286363881
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38482685T>C
(GRCh38)5:38485804C>T
(Homo sapiens)Allele/Variant
Source: rs1259859453
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38485804C>T
(GRCh38)5:38485874A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38485874A>G
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38485874A>G
(GRCh38)5:38485882G>A
(Homo sapiens)Allele/Variant
Source: rs756675225
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38485882G>A
(GRCh38)5:38490283G>A
(Homo sapiens)Allele/Variant
Source: rs199775294
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38490283G>A
(GRCh38)5:38478432A>T
(Homo sapiens)Allele/Variant
Source: rs142495539
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38478432A>T
(GRCh38)5:38479985A>C
(Homo sapiens)Allele/Variant
Source: rs2731964
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38479985A>C
(GRCh38)5:38485805A>C
(Homo sapiens)Allele/Variant
Source: rs541984532
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38485805A>C
(GRCh38)5:38485963C>T
(Homo sapiens)Allele/Variant
Source: rs3110234
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38485963C>T
(GRCh38)5:38489066C>G
(Homo sapiens)Allele/Variant
Source: rs373419706
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38489066C>G
(GRCh38)5:38489077C>T
(Homo sapiens)Allele/Variant
Source: rs772217684
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38489077C>T
(GRCh38)5:38502916C>T
(Homo sapiens)Allele/Variant
Source: rs7701409
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38502916C>T
(GRCh38)5:38503729C>T
(Homo sapiens)Allele/Variant
Source: rs13186262
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38503729C>T
(GRCh38)5:38510522T>A
(Homo sapiens)Allele/Variant
Source: rs2112492126
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38510522T>A
(GRCh38)5:38510548T>C
(Homo sapiens)Allele/Variant
Source: rs772583825
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38510548T>C
(GRCh38)5:38528740A>G
(Homo sapiens)Allele/Variant
Source: rs1022777517
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528740A>G
(GRCh38)5:38528743T>C
(Homo sapiens)Allele/Variant
Source: rs775047163
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528743T>C
(GRCh38)5:38528776T>C
(Homo sapiens)Allele/Variant
Source: rs2112564379
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528776T>C
(GRCh38)5:38528808T>G
(Homo sapiens)Allele/Variant
Source: rs756219488
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528808T>G
(GRCh38)5:38528836A>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38528836A>T
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528836A>T
(GRCh38)5:38528789C>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38528789C>G
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528789C>G
(GRCh38)5:38528797C>A
(Homo sapiens)Allele/Variant
Source: rs1323929710
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38528797C>A
(GRCh38)5:38530561C>A
(Homo sapiens)Allele/Variant
Source: rs1302093251
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38530561C>A
(GRCh38)5:38530639A>C
(Homo sapiens)Allele/Variant
Source: rs746821182
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38530639A>C
(GRCh38)5:38475104T>C
(Homo sapiens)Allele/Variant
Source: rs2112328232
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38475104T>C
(GRCh38)5:38481271C>T
(Homo sapiens)Allele/Variant
Source: rs3797156
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38481271C>T
(GRCh38)5:38503958T>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38503958T>G
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38503958T>G
(GRCh38)5:38504036A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38504036A>G
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38504036A>G
(GRCh38)5:38481740C>G
(Homo sapiens)Allele/Variant
Source: rs1420794475
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38481740C>G
(GRCh38)5:38482003G>A
(Homo sapiens)Allele/Variant
Source: rs775970749
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38482003G>A
(GRCh38)5:38506646A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38506646A>C
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38506646A>C
(GRCh38)5:38506650C>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.38506650C>A
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38506650C>A
(GRCh38)5:38482139A>T
(Homo sapiens)Allele/Variant
Source: rs886060628
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38482139A>T
(GRCh38)5:38510573C>T
(Homo sapiens)Allele/Variant
Source: rs1745742866
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38510573C>T
(GRCh38)5:38479623G>A
(Homo sapiens)Allele/Variant
Source: rs1227741988
Genes: LIFR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:38479623G>A