Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant Molecular Consequence: non coding transcript variant
sa44299
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-9673
Genes: erc1a (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available
Genes: erc1a (Dre)
(GRCh38)12:1115991C>T
(Homo sapiens)Allele/Variant
Source: rs138901829
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1115991C>T
(GRCh38)12:1110209T>A
(Homo sapiens)Allele/Variant
Source: rs36113377
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1110209T>A
(GRCh38)12:1110274G>A
(Homo sapiens)Allele/Variant
Source: rs147857333
Genes: ERC1 (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)12:1110274G>A
(GRCh38)12:1028163G>T
(Homo sapiens)Allele/Variant
Source: rs1225265599
Genes: ERC1 (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)12:1028163G>T
(GRCh38)12:1112269A>G
(Homo sapiens)Allele/Variant
Source: rs150360885
Genes: ERC1 (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)12:1112269A>G
(GRCh38)12:1110325A>G
(Homo sapiens)Allele/Variant
Source: rs372551806
Genes: ERC1 (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)12:1110325A>G
(GRCh38)12:1028200T>G
(Homo sapiens)Allele/Variant
Source: rs146174236
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1028200T>G
(GRCh38)12:1480892G>T
(Homo sapiens)Allele/Variant
Source: rs112807806
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1480892G>T
(GRCh38)12:1083520C>T
(Homo sapiens)Allele/Variant
Source: rs187560506
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1083520C>T
(GRCh38)12:1028211G>C
(Homo sapiens)Allele/Variant
Source: rs535851221
Genes: ERC1 (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)12:1028211G>C
(GRCh38)12:1027951G>C
(Homo sapiens)Allele/Variant
Source: rs61740169
Genes: ERC1 (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)12:1027951G>C
(GRCh38)12:1104765T>G
(Homo sapiens)Allele/Variant
Source: rs758202677
Genes: ERC1 (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)12:1104765T>G
(GRCh38)12:1027988C>T
(Homo sapiens)Allele/Variant
Source: rs1397684571
Genes: ERC1 (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)12:1027988C>T
(GRCh38)12:1110205C>G
(Homo sapiens)Allele/Variant
Source: rs372497149
Genes: ERC1 (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)12:1110205C>G
(GRCh38)12:1104760G>A
(Homo sapiens)Allele/Variant
Source: rs746468698
Genes: ERC1 (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)12:1104760G>A
(GRCh38)12:1083303T>A
(Homo sapiens)Allele/Variant
Source: rs1942496045
Genes: ERC1 (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)12:1083303T>A
(GRCh38)12:1028450A>G
(Homo sapiens)Allele/Variant
Source: rs372323969
Genes: ERC1 (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)12:1028450A>G
(GRCh38)12:1028267A>G
(Homo sapiens)Allele/Variant
Source: rs141356033
Genes: ERC1 (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)12:1028267A>G
(GRCh38)12:1144549A>T
(Homo sapiens)Allele/Variant
Source: rs207472607
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1144549A>T
(GRCh38)12:1083521G>A
(Homo sapiens)Allele/Variant
Source: rs912612332
Genes: ERC1 (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)12:1083521G>A
(GRCh38)12:1028028C>T
(Homo sapiens)Allele/Variant
Source: rs775689550
Genes: ERC1 (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)12:1028028C>T
(GRCh38)12:1180534A>C
(Homo sapiens)Allele/Variant
Source: rs778780521
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1180534A>C
(GRCh38)12:1028423G>A
(Homo sapiens)Allele/Variant
Source: rs1277274163
Genes: ERC1 (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)12:1028423G>A
(GRCh38)12:1027920G>A
(Homo sapiens)Allele/Variant
Source: rs140435811
Genes: ERC1 (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)12:1027920G>A
(GRCh38)12:1189855G>A
(Homo sapiens)Allele/Variant
Source: rs191680119
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1189855G>A
(GRCh38)12:1480847C>T
(Homo sapiens)Allele/Variant
Source: rs11613546
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1480847C>T
(GRCh38)12:1028051A>G
(Homo sapiens)Allele/Variant
Source: rs35037408
Genes: ERC1 (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)12:1028051A>G
(GRCh38)12:1116006G>T
(Homo sapiens)Allele/Variant
Source: rs374949092
Genes: ERC1 (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)12:1116006G>T
(GRCh38)12:1028226G>A
(Homo sapiens)Allele/Variant
Source: rs770130777
Genes: ERC1 (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)12:1028226G>A
(GRCh38)12:1027967C>T
(Homo sapiens)Allele/Variant
Source: rs749881506
Genes: ERC1 (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)12:1027967C>T
(GRCh38)12:1490092G>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.1490092G>A
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1490092G>A
(GRCh38)12:1028203C>T
(Homo sapiens)Allele/Variant
Source: rs138791726
Genes: ERC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:1028203C>T
(mRatBN7.2)4:152962029G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051339.1:g.152962029G>A
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152962029G>A
(mRatBN7.2)4:152962092A>T
(Rattus norvegicus)Allele/Variant
Source: NC_051339.1:g.152962092A>T
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152962092A>T
(mRatBN7.2)4:152962745C>A
(Rattus norvegicus)Allele/Variant
Source: rs3320383922
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152962745C>A
(mRatBN7.2)4:152963747T>G
(Rattus norvegicus)Allele/Variant
Source: rs106433524
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152963747T>G
(mRatBN7.2)4:152970586T>C
(Rattus norvegicus)Allele/Variant
Source: rs65361765
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152970586T>C
(mRatBN7.2)4:152970845T>C
(Rattus norvegicus)Allele/Variant
Source: rs105548900
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152970845T>C
(mRatBN7.2)4:152976943A>T
(Rattus norvegicus)Allele/Variant
Source: rs197051614
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152976943A>T
(mRatBN7.2)4:152977669G>A
(Rattus norvegicus)Allele/Variant
Source: rs3320310244
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152977669G>A
(mRatBN7.2)4:152978223A>C
(Rattus norvegicus)Allele/Variant
Source: rs3320392784
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152978223A>C
(mRatBN7.2)4:152988354A>C
(Rattus norvegicus)Allele/Variant
Source: rs105150922
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152988354A>C
(mRatBN7.2)4:152974473G>T
(Rattus norvegicus)Allele/Variant
Source: rs105311470
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152974473G>T
(mRatBN7.2)4:152988055A>G
(Rattus norvegicus)Allele/Variant
Source: rs198000574
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152988055A>G
(mRatBN7.2)4:152989314T>A
(Rattus norvegicus)Allele/Variant
Source: rs198402026
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152989314T>A
(mRatBN7.2)4:152905809A>C
(Rattus norvegicus)Allele/Variant
Source: rs105030813
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152905809A>C
(mRatBN7.2)4:152907610T>C
(Rattus norvegicus)Allele/Variant
Source: rs104974164
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152907610T>C
(mRatBN7.2)4:152909194C>T
(Rattus norvegicus)Allele/Variant
Source: rs105947355
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152909194C>T
(mRatBN7.2)4:152915637T>G
(Rattus norvegicus)Allele/Variant
Source: NC_051339.1:g.152915637T>G
Genes: Erc1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:152915637T>G