Version: 8.0.0
Date: Tue Jan 28 2025
982 results for lrrc39

(mRatBN7.2)2:204523999C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106191529
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204523999C>T

(mRatBN7.2)2:204525741T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319688915
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204525741T>C

(mRatBN7.2)2:204530172T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319683622
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204530172T>C

(mRatBN7.2)2:204530364A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319679705
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204530364A>G

(mRatBN7.2)2:204531560C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106721958
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531560C>T

(mRatBN7.2)2:204532330C>A

(Rattus norvegicus)
Allele/Variant
Source: rs106008765
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532330C>A

(mRatBN7.2)2:204532444C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106185326
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532444C>T

(mRatBN7.2)2:204532871C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319702082
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532871C>T

(mRatBN7.2)2:204532901C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105794765
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532901C>T

(mRatBN7.2)2:204533321A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319642236
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204533321A>G

(mRatBN7.2)2:204516874C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319692299
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204516874C>A

(mRatBN7.2)2:204517873T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319702264
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204517873T>G

(mRatBN7.2)2:204530358A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319679691
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204530358A>G

(mRatBN7.2)2:204530484G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319678974
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204530484G>A

(mRatBN7.2)2:204531343T>A

(Rattus norvegicus)
Allele/Variant
Source: rs106575181
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531343T>A

(mRatBN7.2)2:204531415C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319681536
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531415C>T

(mRatBN7.2)2:204532179A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319642245
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532179A>G

(mRatBN7.2)2:204532460G>C

(Rattus norvegicus)
Allele/Variant
Source: rs104931019
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532460G>C

(mRatBN7.2)2:204532528G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107262867
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532528G>A

(mRatBN7.2)2:204532545T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105657359
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532545T>C

(mRatBN7.2)2:204532660G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105341840
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532660G>A

(mRatBN7.2)2:204533186C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319690494
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204533186C>T

(mRatBN7.2)2:204521523C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319683552
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204521523C>A

(mRatBN7.2)2:204522104A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319688948
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204522104A>G

(mRatBN7.2)2:204522414G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.204522414G>C
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204522414G>C

(mRatBN7.2)2:204525780A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319642294
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204525780A>C

(mRatBN7.2)2:204528697C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105718600
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528697C>T

(mRatBN7.2)2:204526498C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319642198
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204526498C>T

(mRatBN7.2)2:204527213T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319696740
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204527213T>C

(mRatBN7.2)2:204528773A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319692291
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528773A>G

(mRatBN7.2)2:204525695T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199229351
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204525695T>C

(mRatBN7.2)2:204528639G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106649703
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528639G>A

(GRCh38)1:100148662C>T

(Homo sapiens)
Allele/Variant
Source: rs767533656
Genes: LRRC39 (Hsa), TRMT13 (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)1:100148662C>T

(GRCh38)1:100148785C>T

(Homo sapiens)
Allele/Variant
Source: rs1239467378
Genes: LRRC39 (Hsa), TRMT13 (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)1:100148785C>T

(mRatBN7.2)2:204526682T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105830234
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204526682T>G

(mRatBN7.2)2:204528158T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319642276
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528158T>C

(mRatBN7.2)2:204528660G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319659816
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204528660G>A

(mRatBN7.2)2:204531132C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319610072
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531132C>T

(mRatBN7.2)2:204531358T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319696800
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531358T>G

(mRatBN7.2)2:204531360G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105210744
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204531360G>A

(mRatBN7.2)2:204532586G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198333518
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532586G>A

(mRatBN7.2)2:204532674T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106163213
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532674T>C

(mRatBN7.2)2:204532743C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105658783
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204532743C>T

(mRatBN7.2)2:204533067G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319702222
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204533067G>A

(mRatBN7.2)2:204517637G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051337.1:g.204517637G>A
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204517637G>A

(mRatBN7.2)2:204519783C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319696701
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204519783C>T

(mRatBN7.2)2:204520053C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319692218
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204520053C>T

(mRatBN7.2)2:204520463C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198861540
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204520463C>T

(mRatBN7.2)2:204521930G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198338403
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204521930G>A

(mRatBN7.2)2:204522855C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319657097
Genes: Lrrc39 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:204522855C>T