Version: 8.1.0
Date: Fri Apr 18 2025
327 results for scrt2

(GRCh38)20:664186C>T

(Homo sapiens)
Allele/Variant
Source: rs1984070156
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664186C>T

(GRCh38)20:664200G>A

(Homo sapiens)
Allele/Variant
Source: rs1244777883
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664200G>A

(GRCh38)20:664375G>A

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.664375G>A
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664375G>A

(GRCh38)20:664243A>C

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.664243A>C
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664243A>C

(GRCh38)20:664287G>T

(Homo sapiens)
Allele/Variant
Source: rs368666776
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664287G>T

(GRCh38)20:675504A>G

(Homo sapiens)
Allele/Variant
Source: rs1289880415
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:675504A>G

(GRCh38)20:675540G>A

(Homo sapiens)
Allele/Variant
Source: rs762554724
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:675540G>A

(GRCh38)20:663779C>G

(Homo sapiens)
Allele/Variant
Source: rs201413966
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:663779C>G

(GRCh38)20:664152T>G

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.664152T>G
Genes: SCRT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:664152T>G

(mRatBN7.2)3:140584274T>G

(Rattus norvegicus)
Allele/Variant
Source: rs198556664
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140584274T>G

(mRatBN7.2)3:140587048C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197678931
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140587048C>T

(GRCm39)2:151934912G>A

(Mus musculus)
Allele/Variant
Source: rs29963018
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151934912G>A

(GRCm39)2:151935404C>T

(Mus musculus)
Allele/Variant
Source: rs237347937
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151935404C>T

(GRCm39)2:151925463A>G

(Mus musculus)
Allele/Variant
Source: rs254808571
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151925463A>G

(GRCm39)2:151936289A>C

(Mus musculus)
Allele/Variant
Source: rs258788939
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151936289A>C

(GRCm39)2:151925936G>C

(Mus musculus)
Allele/Variant
Source: rs246574607
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151925936G>C

(GRCm39)2:151928105A>T

(Mus musculus)
Allele/Variant
Source: rs234639537
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151928105A>T

(GRCm39)2:151930731C>T

(Mus musculus)
Allele/Variant
Source: rs33199900
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151930731C>T

(GRCm39)2:151931114G>A

(Mus musculus)
Allele/Variant
Source: rs219662074
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151931114G>A

(mRatBN7.2)3:140591174A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140591174A>T
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140591174A>T

(mRatBN7.2)3:140593798C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140593798C>T
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140593798C>T

(mRatBN7.2)3:140593800C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140593800C>T
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140593800C>T

(GRCm39)2:151933563G>A

(Mus musculus)
Allele/Variant
Source: rs225027788
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151933563G>A

(GRCm39)2:151935070G>A

(Mus musculus)
Allele/Variant
Source: rs219022363
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151935070G>A

(GRCm39)2:151935616C>T

(Mus musculus)
Allele/Variant
Source: rs222630462
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151935616C>T

(GRCm39)2:151936269A>G

(Mus musculus)
Allele/Variant
Source: rs584495925
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151936269A>G

(GRCm39)2:151925514A>C

(Mus musculus)
Allele/Variant
Source: rs237519991
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151925514A>C

(GRCm39)2:151928134T>A

(Mus musculus)
Allele/Variant
Source: rs247704403
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151928134T>A

(GRCm39)2:151928135T>A

(Mus musculus)
Allele/Variant
Source: rs212496677
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151928135T>A

(mRatBN7.2)3:140594007T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198029923
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140594007T>C

(mRatBN7.2)3:140583933C>T

(Rattus norvegicus)
Allele/Variant
Source: rs196965405
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140583933C>T

(mRatBN7.2)3:140586497A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198098237
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140586497A>G

(mRatBN7.2)3:140592113A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199072208
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140592113A>G

(mRatBN7.2)3:140592117G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140592117G>A
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140592117G>A

(mRatBN7.2)3:140584082A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197460646
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140584082A>G

(GRCm39)2:151933838A>G

(Mus musculus)
Allele/Variant
Source: rs47600101
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151933838A>G

(GRCm39)2:151923586G>C

(Mus musculus)
Allele/Variant
Source: rs231128177
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151923586G>C

(GRCm39)2:151923775C>T

(Mus musculus)
Allele/Variant
Source: rs582742131
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151923775C>T

(GRCm39)2:151932735A>T

(Mus musculus)
Allele/Variant
Source: rs51601486
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151932735A>T

(mRatBN7.2)3:140584422T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140584422T>A
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140584422T>A

(mRatBN7.2)3:140589754T>G

(Rattus norvegicus)
Allele/Variant
Source: rs199339683
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140589754T>G

(mRatBN7.2)3:140592484T>C

(Rattus norvegicus)
Allele/Variant
Source: rs196980541
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140592484T>C

(mRatBN7.2)3:140591170T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.140591170T>A
Genes: Scrt2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:140591170T>A

(GRCm39)2:151935001G>A

(Mus musculus)
Allele/Variant
Source: rs33624806
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151935001G>A

(GRCm39)2:151924135T>C

(Mus musculus)
Allele/Variant
Source: rs248702706
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151924135T>C

(GRCm39)2:151935607A>G

(Mus musculus)
Allele/Variant
Source: rs265311962
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151935607A>G

(GRCm39)2:151932926A>C

(Mus musculus)
Allele/Variant
Source: rs46640618
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151932926A>C

(GRCm39)2:151927707C>T

(Mus musculus)
Allele/Variant
Source: rs235805702
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151927707C>T

(GRCm39)2:151930467C>T

(Mus musculus)
Allele/Variant
Source: rs249055350
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151930467C>T

(GRCm39)2:151932403A>T

(Mus musculus)
Allele/Variant
Source: rs217379090
Genes: Scrt2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:151932403A>T