Version: 8.1.0
Date: Fri Apr 18 2025
1,998 results for nipa1
Allele/Variant

Nipa1tm1a(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4363744
Genes: Nipa1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nipa1 (Mmu)
Genes: Nipa1 (Mmu)
Symbol: Nipa1tm1a(KOMP)Wtsi

Nipa1em10Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7303030
Genes: Nipa1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nipa1 (Mmu)
Genes: Nipa1 (Mmu)
Symbol: Nipa1em10Gpt

Nipa1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7303031
Genes: Nipa1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nipa1 (Mmu)
Genes: Nipa1 (Mmu)
Symbol: Nipa1em1Gpt

Nipa1tm1Osb

(Mus musculus)
Allele/Variant
Source: MGI:7341592
Genes: Nipa1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Nipa1 (Mmu)
Genes: Nipa1 (Mmu)
Symbol: Nipa1tm1Osb

uab382

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-220322-35
Genes: nipa1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: nipa1 (Dre)

(GRCh38)15:22812228C>A

(Homo sapiens)
Allele/Variant
Source: rs1235395631
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812228C>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786776G>C

(Homo sapiens)
Allele/Variant
Source: rs1369223854
Genes: NIPA1 (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)15:22786776G>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786782C>T

(Homo sapiens)
Allele/Variant
Source: rs748012969
Genes: NIPA1 (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)15:22786782C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812443C>G

(Homo sapiens)
Allele/Variant
Source: rs7168401
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812443C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786669G>T

(Homo sapiens)
Allele/Variant
Source: rs976686334
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22786669G>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22824143C>T

(Homo sapiens)
Allele/Variant
Source: rs1555374032
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22824143C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22810786C>G

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.22810786C>G
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22810786C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823757C>G

(Homo sapiens)
Allele/Variant
Source: rs1895592461
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823757C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823760A>T

(Homo sapiens)
Allele/Variant
Source: rs762651676
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823760A>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823789G>A

(Homo sapiens)
Allele/Variant
Source: rs761905589
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823789G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786816G>C

(Homo sapiens)
Allele/Variant
Source: rs2140841523
Genes: NIPA1 (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)15:22786816G>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22810537G>C

(Homo sapiens)
Allele/Variant
Source: rs117974214
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22810537G>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823699C>T

(Homo sapiens)
Allele/Variant
Source: rs12592629
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823699C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823717C>T

(Homo sapiens)
Allele/Variant
Source: rs2140877624
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823717C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786701G>A

(Homo sapiens)
Allele/Variant
Source: rs1555371616
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22786701G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22825516A>C

(Homo sapiens)
Allele/Variant
Source: rs1045487020
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22825516A>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22826704C>G

(Homo sapiens)
Allele/Variant
Source: rs1191576484
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22826704C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22824050G>T

(Homo sapiens)
Allele/Variant
Source: rs185222838
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22824050G>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823450T>C

(Homo sapiens)
Allele/Variant
Source: rs184154944
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823450T>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823822C>T

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.22823822C>T
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823822C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786786T>G

(Homo sapiens)
Allele/Variant
Source: rs1595626779
Genes: NIPA1 (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)15:22786786T>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22820627C>T

(Homo sapiens)
Allele/Variant
Source: rs59940862
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22820627C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823708G>C

(Homo sapiens)
Allele/Variant
Source: rs372189145
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823708G>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823719G>A

(Homo sapiens)
Allele/Variant
Source: rs1566789035
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823719G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812252G>A

(Homo sapiens)
Allele/Variant
Source: rs104894490
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812252G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22820298C>T

(Homo sapiens)
Allele/Variant
Source: rs1555373770
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22820298C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22820404A>G

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.22820404A>G
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22820404A>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22827366G>A

(Homo sapiens)
Allele/Variant
Source: rs547238314
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22827366G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22827517C>G

(Homo sapiens)
Allele/Variant
Source: rs57615013
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22827517C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22827701A>G

(Homo sapiens)
Allele/Variant
Source: rs766376279
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22827701A>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22810959C>T

(Homo sapiens)
Allele/Variant
Source: rs17137329
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22810959C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812211C>T

(Homo sapiens)
Allele/Variant
Source: rs765306724
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812211C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812235C>T

(Homo sapiens)
Allele/Variant
Source: rs1356799862
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812235C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823760A>G

(Homo sapiens)
Allele/Variant
Source: rs762651676
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823760A>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823876C>T

(Homo sapiens)
Allele/Variant
Source: rs759267223
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823876C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812252G>C

(Homo sapiens)
Allele/Variant
Source: rs104894490
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812252G>C
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22812266A>G

(Homo sapiens)
Allele/Variant
Source: rs372614917
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22812266A>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22827941C>T

(Homo sapiens)
Allele/Variant
Source: rs3812923
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22827941C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22825942C>T

(Homo sapiens)
Allele/Variant
Source: rs763790822
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22825942C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22829424C>T

(Homo sapiens)
Allele/Variant
Source: rs569739849
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22829424C>T
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22786746C>G

(Homo sapiens)
Allele/Variant
Source: rs776212895
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22786746C>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22824770T>G

(Homo sapiens)
Allele/Variant
Source: rs1020166733
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22824770T>G
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22828242G>A

(Homo sapiens)
Allele/Variant
Source: rs1452895080
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22828242G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22829203G>A

(Homo sapiens)
Allele/Variant
Source: rs146129067
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22829203G>A
Gene Synonyms: magnesium transporter NIPA1

(GRCh38)15:22823950T>C

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.22823950T>C
Genes: NIPA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)15:22823950T>C
Gene Synonyms: magnesium transporter NIPA1