Version: 8.0.0
Date: Tue Jan 28 2025
6,445 results for lrriq1

(GRCh38)12:85056817A>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85056817A>G
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056817A>G

(GRCh38)12:85056901C>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85056901C>G
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056901C>G

(GRCh38)12:85056190A>G

(Homo sapiens)
Allele/Variant
Source: rs1301221845
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056190A>G

(GRCh38)12:85038211T>C

(Homo sapiens)
Allele/Variant
Source: rs766219757
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85038211T>C

(GRCh38)12:85046086G>A

(Homo sapiens)
Allele/Variant
Source: rs149503974
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85046086G>A

(GRCh38)12:85038190A>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85038190A>T
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85038190A>T

(GRCh38)12:85055721C>G

(Homo sapiens)
Allele/Variant
Source: rs201694390
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85055721C>G

(GRCh38)12:85066764C>A

(Homo sapiens)
Allele/Variant
Source: rs147534931
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85066764C>A

(GRCh38)12:85124327C>T

(Homo sapiens)
Allele/Variant
Source: rs377176302
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124327C>T

(GRCh38)12:85124131C>G

(Homo sapiens)
Allele/Variant
Source: rs770626027
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124131C>G

(GRCh38)12:85098940C>T

(Homo sapiens)
Allele/Variant
Source: rs1438535984
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85098940C>T

(GRCh38)12:85124429G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85124429G>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124429G>C

(GRCh38)12:85160670A>T

(Homo sapiens)
Allele/Variant
Source: rs766067329
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85160670A>T

(GRCh38)12:85229625C>T

(Homo sapiens)
Allele/Variant
Source: rs375186528
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85229625C>T

(GRCh38)12:85056525A>C

(Homo sapiens)
Allele/Variant
Source: rs758484541
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056525A>C

(GRCh38)12:85056385A>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85056385A>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056385A>C

(GRCh38)12:85056978G>A

(Homo sapiens)
Allele/Variant
Source: rs775456418
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056978G>A

(GRCh38)12:85057019A>C

(Homo sapiens)
Allele/Variant
Source: rs1351643627
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85057019A>C

(GRCh38)12:85121865A>G

(Homo sapiens)
Allele/Variant
Source: rs1461413215
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85121865A>G

(GRCh38)12:85124426G>A

(Homo sapiens)
Allele/Variant
Source: rs1482214955
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124426G>A

(GRCh38)12:85153095T>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85153095T>G
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85153095T>G

(GRCh38)12:85153674A>G

(Homo sapiens)
Allele/Variant
Source: rs1462325478
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85153674A>G

(GRCh38)12:85065275C>A

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85065275C>A
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85065275C>A

(GRCh38)12:85038217C>T

(Homo sapiens)
Allele/Variant
Source: rs200816060
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85038217C>T

(GRCh38)12:85046032A>G

(Homo sapiens)
Allele/Variant
Source: rs774053980
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85046032A>G

(GRCh38)12:85047299G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85047299G>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85047299G>C

(GRCh38)12:85056771A>G

(Homo sapiens)
Allele/Variant
Source: rs1881141451
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056771A>G

(GRCh38)12:85121863A>G

(Homo sapiens)
Allele/Variant
Source: rs766184197
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85121863A>G

(GRCh38)12:85124417G>A

(Homo sapiens)
Allele/Variant
Source: rs377703986
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124417G>A

(GRCh38)12:85127918C>T

(Homo sapiens)
Allele/Variant
Source: rs749863431
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85127918C>T

(GRCh38)12:85124077T>C

(Homo sapiens)
Allele/Variant
Source: rs374288998
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124077T>C

(GRCh38)12:85229550C>T

(Homo sapiens)
Allele/Variant
Source: rs754318985
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85229550C>T

(GRCh38)12:85244882G>A

(Homo sapiens)
Allele/Variant
Source: rs773114283
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85244882G>A

(GRCh38)12:85124165G>T

(Homo sapiens)
Allele/Variant
Source: rs367637593
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124165G>T

(GRCh38)12:85127836G>A

(Homo sapiens)
Allele/Variant
Source: rs748072772
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85127836G>A

(GRCh38)12:85177975G>A

(Homo sapiens)
Allele/Variant
Source: rs207473208
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85177975G>A

(GRCh38)12:85098438C>A

(Homo sapiens)
Allele/Variant
Source: rs200596040
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85098438C>A

(GRCh38)12:85137863G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85137863G>C
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85137863G>C

(GRCh38)12:85137937G>A

(Homo sapiens)
Allele/Variant
Source: rs915880508
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85137937G>A

(GRCh38)12:85154058C>G

(Homo sapiens)
Allele/Variant
Source: rs778415975
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85154058C>G

(GRCh38)12:85106538A>G

(Homo sapiens)
Allele/Variant
Source: rs75325032
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85106538A>G

(GRCh38)12:85124225C>A

(Homo sapiens)
Allele/Variant
Source: rs775555011
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124225C>A

(GRCh38)12:85124122T>A

(Homo sapiens)
Allele/Variant
Source: rs1472234240
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124122T>A

(GRCh38)12:85056750A>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.85056750A>G
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85056750A>G

(GRCh38)12:85072913C>T

(Homo sapiens)
Allele/Variant
Source: rs773796685
Genes: LRRIQ1 (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)12:85072913C>T

(GRCh38)12:85121722G>A

(Homo sapiens)
Allele/Variant
Source: rs147080103
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85121722G>A

(GRCh38)12:85121762C>T

(Homo sapiens)
Allele/Variant
Source: rs1393488672
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85121762C>T

(GRCh38)12:85124229C>A

(Homo sapiens)
Allele/Variant
Source: rs1252810004
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85124229C>A

(GRCh38)12:85168364T>C

(Homo sapiens)
Allele/Variant
Source: rs207473207
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85168364T>C

(GRCh38)12:85154071C>T

(Homo sapiens)
Allele/Variant
Source: rs758802431
Genes: LRRIQ1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:85154071C>T