Version: 8.0.0
Date: Tue Jan 28 2025
672 results for wdcp

(mRatBN7.2)6:27864358G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320773811
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27864358G>A

(mRatBN7.2)6:27862874T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320770064
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27862874T>G

(mRatBN7.2)6:27864198A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320784283
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27864198A>G

(mRatBN7.2)6:27857410G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320686225
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27857410G>C

(mRatBN7.2)6:27860158G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320810764
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27860158G>A

(mRatBN7.2)6:27854194T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051341.1:g.27854194T>C
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27854194T>C

(mRatBN7.2)6:27854204T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051341.1:g.27854204T>C
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27854204T>C

(mRatBN7.2)6:27850784G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320824843
Genes: Wdcp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:27850784G>A

(GRCm39)12:4907733C>T

(Mus musculus)
Allele/Variant
Source: rs47998116
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4907733C>T

(GRCm39)12:4892819G>T

(Mus musculus)
Allele/Variant
Source: rs580638398
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4892819G>T

(GRCm39)12:4893020C>T

(Mus musculus)
Allele/Variant
Source: rs579205114
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893020C>T

(GRCm39)12:4893232G>A

(Mus musculus)
Allele/Variant
Source: rs260458404
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893232G>A

(GRCm39)12:4903513C>G

(Mus musculus)
Allele/Variant
Source: rs260123000
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903513C>G

(GRCm39)12:4903606C>T

(Mus musculus)
Allele/Variant
Source: rs247667702
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903606C>T

(GRCm39)12:4903612C>T

(Mus musculus)
Allele/Variant
Source: rs47322077
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903612C>T

(GRCm39)12:4903637G>A

(Mus musculus)
Allele/Variant
Source: rs262701538
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903637G>A

(GRCm39)12:4903689A>G

(Mus musculus)
Allele/Variant
Source: rs230177691
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903689A>G

(GRCm39)12:4903710G>A

(Mus musculus)
Allele/Variant
Source: rs587234280
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903710G>A

(GRCm39)12:4903728C>T

(Mus musculus)
Allele/Variant
Source: rs213664877
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903728C>T

(GRCm39)12:4903746T>G

(Mus musculus)
Allele/Variant
Source: rs216921750
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903746T>G

(GRCm39)12:4903801G>T

(Mus musculus)
Allele/Variant
Source: rs237625684
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903801G>T

(GRCm39)12:4904798C>A

(Mus musculus)
Allele/Variant
Source: rs215774959
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4904798C>A

(GRCm39)12:4905045C>T

(Mus musculus)
Allele/Variant
Source: rs582456291
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4905045C>T

(GRCm39)12:4906024C>A

(Mus musculus)
Allele/Variant
Source: rs212925246
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4906024C>A

(GRCm39)12:4906315G>T

(Mus musculus)
Allele/Variant
Source: rs1132002033
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4906315G>T

(GRCm39)12:4906393T>C

(Mus musculus)
Allele/Variant
Source: rs250926512
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4906393T>C

(GRCm39)12:4908883T>C

(Mus musculus)
Allele/Variant
Source: rs251135709
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4908883T>C

(GRCm39)12:4909691G>A

(Mus musculus)
Allele/Variant
Source: rs253560885
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4909691G>A

(GRCm39)12:4903325G>C

(Mus musculus)
Allele/Variant
Source: rs1135141780
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903325G>C

(GRCm39)12:4903439T>C

(Mus musculus)
Allele/Variant
Source: rs223557482
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4903439T>C

(GRCm39)12:4904990A>C

(Mus musculus)
Allele/Variant
Source: rs248045442
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4904990A>C

(GRCm39)12:4906377G>C

(Mus musculus)
Allele/Variant
Source: rs238103131
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4906377G>C

(GRCm39)12:4896882G>A

(Mus musculus)
Allele/Variant
Source: rs246418773
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4896882G>A

(GRCm39)12:4895026C>A

(Mus musculus)
Allele/Variant
Source: rs237998005
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895026C>A

(GRCm39)12:4895146C>T

(Mus musculus)
Allele/Variant
Source: rs221262695
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895146C>T

(GRCm39)12:4895155C>T

(Mus musculus)
Allele/Variant
Source: rs250714108
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895155C>T

(GRCm39)12:4895247T>C

(Mus musculus)
Allele/Variant
Source: rs245421153
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895247T>C

(GRCm39)12:4895300G>A

(Mus musculus)
Allele/Variant
Source: rs580455872
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895300G>A

(GRCm39)12:4895451A>G

(Mus musculus)
Allele/Variant
Source: rs214243249
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895451A>G

(GRCm39)12:4895452C>T

(Mus musculus)
Allele/Variant
Source: rs229918523
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895452C>T

(GRCm39)12:4902156G>T

(Mus musculus)
Allele/Variant
Source: rs47022969
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4902156G>T

(GRCm39)12:4897574A>G

(Mus musculus)
Allele/Variant
Source: rs219557204
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4897574A>G

(GRCm39)12:4899577T>A

(Mus musculus)
Allele/Variant
Source: rs584535153
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4899577T>A

(GRCm39)12:4893414G>A

(Mus musculus)
Allele/Variant
Source: rs256411385
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893414G>A

(GRCm39)12:4893751C>T

(Mus musculus)
Allele/Variant
Source: rs261850669
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893751C>T

(GRCm39)12:4893791G>T

(Mus musculus)
Allele/Variant
Source: rs219801247
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893791G>T

(GRCm39)12:4893980C>A

(Mus musculus)
Allele/Variant
Source: rs585294840
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4893980C>A

(GRCm39)12:4894543T>A

(Mus musculus)
Allele/Variant
Source: rs48518287
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4894543T>A

(GRCm39)12:4895907A>G

(Mus musculus)
Allele/Variant
Source: rs586477464
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895907A>G

(GRCm39)12:4895985G>A

(Mus musculus)
Allele/Variant
Source: rs580819056
Genes: Wdcp (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:4895985G>A