Version: 8.0.0Date: Tue Jan 28 2025
Category
(GRCh38)6:138096471T>C
(Homo sapiens)Allele/Variant
Source: rs144266393
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138096471T>C
(GRCh38)6:138092158C>T
(Homo sapiens)Allele/Variant
Source: rs1775596006
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138092158C>T
Gene Ontology
Source: GO:0006915
Synonyms:
- activation of apoptosis
- apoptosis
Branch: biological process
Genes: PERP (Hsa)...perp (Dre)
(GRCh38)6:138092171C>T
(Homo sapiens)Allele/Variant
Source: rs1775596924
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)6:138092171C>T
(GRCh38)6:138107166C>T
(Homo sapiens)Allele/Variant
Source: rs146568280
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107166C>T
(GRCh38)6:138092232A>G
(Homo sapiens)Allele/Variant
Source: rs541396173
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138092232A>G
(GRCh38)6:138107271C>A
(Homo sapiens)Allele/Variant
Source: rs79571603
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107271C>A
(GRCh38)6:138092172C>T
(Homo sapiens)Allele/Variant
Source: rs1775596990
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)6:138092172C>T
(GRCh38)6:138107131C>G
(Homo sapiens)Allele/Variant
Source: rs376957775
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107131C>G
(GRCh38)6:138092165G>C
(Homo sapiens)Allele/Variant
Source: rs201454106
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)6:138092165G>C
(GRCh38)6:138096415G>A
(Homo sapiens)Allele/Variant
Source: rs61730263
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138096415G>A
(GRCh38)6:138107216C>A
(Homo sapiens)Allele/Variant
Source: rs78795891
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107216C>A
(GRCh38)6:138096400C>A
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.138096400C>A
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138096400C>A
(GRCh38)6:138096479G>A
(Homo sapiens)Allele/Variant
Source: rs545423525
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138096479G>A
(GRCh38)6:138107241C>T
(Homo sapiens)Allele/Variant
Source: rs1238585676
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107241C>T
(GRCh38)6:138107242G>A
(Homo sapiens)Allele/Variant
Source: rs145663845
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138107242G>A
(GRCh38)6:138092165G>T
(Homo sapiens)Allele/Variant
Source: rs201454106
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)6:138092165G>T
(GRCh38)6:138092236G>A
(Homo sapiens)Allele/Variant
Source: rs200654686
Genes: PERP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)6:138092236G>A
Gene Ontology
Source: GO:0005794
Synonyms:
- Golgi
- Golgi complex
Branch: cellular component
Genes: Perp (Mmu)...Perp (Rno)...PERP (Hsa)
(mRatBN7.2)1:13545111G>A
(Rattus norvegicus)Allele/Variant
Source: rs197619255
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13545111G>A
(mRatBN7.2)1:13542681C>T
(Rattus norvegicus)Allele/Variant
Source: rs3318837111
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13542681C>T
(mRatBN7.2)1:13543136G>A
(Rattus norvegicus)Allele/Variant
Source: rs197339056
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13543136G>A
(mRatBN7.2)1:13543195C>A
(Rattus norvegicus)Allele/Variant
Source: rs198591844
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13543195C>A
(mRatBN7.2)1:13543420C>T
(Rattus norvegicus)Allele/Variant
Source: rs197883773
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13543420C>T
(mRatBN7.2)1:13546073A>G
(Rattus norvegicus)Allele/Variant
Source: rs3318835730
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13546073A>G
(mRatBN7.2)1:13546160T>C
(Rattus norvegicus)Allele/Variant
Source: rs198382222
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13546160T>C
(mRatBN7.2)1:13547425C>T
(Rattus norvegicus)Allele/Variant
Source: rs199233472
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13547425C>T
(mRatBN7.2)1:13550288G>A
(Rattus norvegicus)Allele/Variant
Source: rs3318834874
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550288G>A
(mRatBN7.2)1:13550335G>A
(Rattus norvegicus)Allele/Variant
Source: rs3318835091
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550335G>A
(mRatBN7.2)1:13546979C>T
(Rattus norvegicus)Allele/Variant
Source: rs197226514
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13546979C>T
(mRatBN7.2)1:13547028T>C
(Rattus norvegicus)Allele/Variant
Source: rs199398742
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13547028T>C
(mRatBN7.2)1:13548536C>T
(Rattus norvegicus)Allele/Variant
Source: rs199285232
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13548536C>T
(mRatBN7.2)1:13549179C>A
(Rattus norvegicus)Allele/Variant
Source: rs197956609
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13549179C>A
(mRatBN7.2)1:13550506A>G
(Rattus norvegicus)Allele/Variant
Source: rs3318835988
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550506A>G
(mRatBN7.2)1:13550535T>C
(Rattus norvegicus)Allele/Variant
Source: rs3318835931
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550535T>C
(mRatBN7.2)1:13551203A>G
(Rattus norvegicus)Allele/Variant
Source: rs3318835776
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13551203A>G
(mRatBN7.2)1:13552038G>A
(Rattus norvegicus)Allele/Variant
Source: rs3318835958
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13552038G>A
(mRatBN7.2)1:13553336G>C
(Rattus norvegicus)Allele/Variant
Source: rs8148146
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13553336G>C
(mRatBN7.2)1:13549088G>A
(Rattus norvegicus)Allele/Variant
Source: rs198972184
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13549088G>A
(mRatBN7.2)1:13549444G>A
(Rattus norvegicus)Allele/Variant
Source: rs3318835954
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13549444G>A
(mRatBN7.2)1:13542547C>A
(Rattus norvegicus)Allele/Variant
Source: rs197152695
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13542547C>A
(mRatBN7.2)1:13543686G>A
(Rattus norvegicus)Allele/Variant
Source: rs197088241
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13543686G>A
(mRatBN7.2)1:13546710G>A
(Rattus norvegicus)Allele/Variant
Source: rs198282694
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13546710G>A
(mRatBN7.2)1:13543340A>G
(Rattus norvegicus)Allele/Variant
Source: rs199392227
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13543340A>G
(mRatBN7.2)1:13551843A>C
(Rattus norvegicus)Allele/Variant
Source: rs3318836052
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13551843A>C
(mRatBN7.2)1:13544270G>C
(Rattus norvegicus)Allele/Variant
Source: rs197486364
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13544270G>C
(mRatBN7.2)1:13550771G>A
(Rattus norvegicus)Allele/Variant
Source: rs3318836793
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550771G>A
(mRatBN7.2)1:13550998A>G
(Rattus norvegicus)Allele/Variant
Source: rs3318833544
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13550998A>G
(mRatBN7.2)1:13553240G>T
(Rattus norvegicus)Allele/Variant
Source: rs8148304
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13553240G>T
(mRatBN7.2)1:13546076A>T
(Rattus norvegicus)Allele/Variant
Source: rs3318834180
Genes: Perp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:13546076A>T