132489852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: 110596667-G-A

132489870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: 110596649-C-T

132489892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: 110596629-T-A

132489892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: 110596629-T-C

http://identifiers.org/hco/12/GRCh38#132490006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110596501-A-C

132490022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5 prime UTR variant
orthologous variants: 110596485-C-T

132490233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110596283-G-A

132490233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110596283-G-C

132490233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110596283-G-T

132490333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110596218-G-A

132490393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110596166-C-G

132490397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110596162-G-T

http://identifiers.org/hco/12/GRCh38#132490420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110596143-C-A

132490420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110596143-C-T

132490524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 110596067-G-A

132490946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595686-G-A

132490946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595686-G-T

132491006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595668-T-C

132491011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595663-G-A

132491011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595663-G-T

132491213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595549-G-C

132491213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595549-G-T

132491218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595539-G-C

132491584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595158-T-G

132491755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110595007-C-G

132502318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110586069-C-T

132502390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110586002-C-G

132502390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110586002-C-T

132508036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581072-G-A

132508036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581072-G-C

132508036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581072-G-T

132508037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581071-A-G

132508046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581062-T-C

132508065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581042-T-C

132508077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110581027-G-A

132508130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110580988-G-T

132508171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110580947-C-T

132508252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110580866-A-G

132509064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110580105-G-A

132509064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110580105-G-T

132509132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110580043-G-A

132509132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110580043-G-T

132509189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110579986-G-A

132509189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110579986-G-C

132509189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110579986-G-T

132509341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110579855-T-C

132509401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110579795-G-A

132509401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110579795-G-T

132509409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110579787-C-T

http://identifiers.org/hco/12/GRCh38#132509892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110579388-C-A

132509892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110579388-C-T

132510095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110579185-G-A

132510095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110579185-G-T

132510114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110579166-C-T

http://identifiers.org/hco/12/GRCh38#132510453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110578839-C-A

132510453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578839-C-G

132510453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578839-C-T

http://identifiers.org/hco/12/GRCh38#132510776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110578600-C-A

132510776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578600-C-T

132510788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578588-G-A

132510826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578549-G-A

132510826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578549-G-C

132510826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578549-G-T

132510837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578538-T-C

132510914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578482-C-G

http://identifiers.org/hco/12/GRCh38#132511070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110578311-C-A

132511070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578311-C-T

132511073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578310-G-A

132511073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578310-G-T

132511118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578265-G-A

132511118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578265-G-T

132511212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578194-T-A

http://identifiers.org/hco/12/GRCh38#132511272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110578168-C-A

132511272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578168-C-G

132511272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578168-C-T

132511325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578125-T-C

132511432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578033-G-A

132511432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578033-G-T

132511462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578005-G-A

132511462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110578005-G-T

132511512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110577960-A-G

http://identifiers.org/hco/12/GRCh38#132512005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110577688-C-A

132512005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110577688-C-G

132512016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110577677-C-G

132512016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110577677-C-T

132516896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110573451-C-T

132517071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110573207-C-T

132525690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110565854-G-T

http://identifiers.org/hco/12/GRCh38#132525833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110565697-C-A

132525833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110565697-C-T

132526179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110565122-G-T

http://identifiers.org/hco/12/GRCh38#132528050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110563834-A-C

132528050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110563834-A-G

132528050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110563834-A-T

132528457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110563549-G-A

132528891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110563283-T-A

132529007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110563227-A-G

132530555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110561777-C-G

132530764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110561595-C-T

132530941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110561449-T-C

132531060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110561341-G-A

132532947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110557029-C-T

132533073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110556892-G-A

132533093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110556872-C-T

http://identifiers.org/hco/12/GRCh38#132533122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110556841-C-A

132533122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110556841-C-T

132535030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110554570-G-A

132535075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110554522-C-T

132535155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110554439-T-C

132535242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110554356-C-T

132544900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110547023-T-A

132544900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110547023-T-C

http://identifiers.org/hco/12/GRCh38#132544949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110546943-C-A

132544997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546904-C-G

132544997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546904-C-T

132545305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546689-G-A

132545340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546656-T-C

132545382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546614-G-C

132545442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546562-G-A

132545540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110546473-T-G

http://identifiers.org/hco/12/GRCh38#132545658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#110546372-A-C

132545658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, undefined
orthologous variants: 110546372-A-G

132545658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, undefined
orthologous variants: 110546372-A-T

http://identifiers.org/hco/12/GRCh38#132545694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110546350-C-A

132546706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110545073-G-A

132546825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110545026-T-C

132546857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544994-G-A

132546977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544870-C-T

132547166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544683-G-A

132547571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544316-C-T

132547703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544191-T-C

132547885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544040-T-A

132547885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544040-T-C

http://identifiers.org/hco/12/GRCh38#132547913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110544023-C-A

132547913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544023-C-T

132547929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544007-G-A

132547929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110544007-G-T

http://identifiers.org/hco/12/GRCh38#132548075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110543882-C-A

132548075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110543882-C-T

132551601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541158-G-T

132551679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541071-A-G

http://identifiers.org/hco/12/GRCh38#132551690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110541059-C-A

132551690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541059-C-T

http://identifiers.org/hco/12/GRCh38#132551695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110541054-C-A

http://identifiers.org/hco/12/GRCh38#132551700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110541049-C-A

132551700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541049-C-G

132551705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541038-A-G

132551705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541038-A-T

132551718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541016-A-G

132551719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541015-G-A

132551719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110541015-G-T

132557203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110537267-G-A

132557317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110537154-G-A

132557317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110537154-G-T

132557462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110537003-C-T

132557484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110536981-G-A

http://identifiers.org/hco/12/GRCh38#132557488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110536977-C-A

132557488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110536977-C-T

132558697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110535769-G-A

http://identifiers.org/hco/12/GRCh38#132560041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110534967-C-A

132560041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110534967-C-T

132560101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110534899-G-A

132560101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110534899-G-C

132560101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110534899-G-T

132560135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110534867-G-A

132560135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110534867-G-C

132560135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110534867-G-T

132560672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110534346-G-A

132560672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110534346-G-T

132560758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110534267-C-T

http://identifiers.org/hco/12/GRCh38#132569870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110527513-A-C

132569870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110527513-A-G

132569870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110527513-A-T

132569871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110527512-G-A

132569871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110527512-G-T

132570006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110527374-G-A

132570006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110527374-G-T

132570009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110527371-G-A

132570009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110527371-G-T

132570073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110527322-G-A

132570073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110527322-G-T

http://identifiers.org/hco/12/GRCh38#132570141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110527251-C-A

132570141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110527251-C-T

132570195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110527197-T-A

132570195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110527197-T-C

132570272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110527056-T-A

132570287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110527036-G-A

132570287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110527036-G-T

http://identifiers.org/hco/12/GRCh38#132570323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110526990-C-A

132570323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526990-C-T

http://identifiers.org/hco/12/GRCh38#132570549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110526749-C-A

132570560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526730-T-A

132570609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526703-G-A

132570815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526575-A-G

http://identifiers.org/hco/12/GRCh38#132570919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110526486-C-A

132570919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526486-C-G

132570919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526486-C-T

132570994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526415-C-T

132571011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526411-G-A

132571011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526411-G-T

132571016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526406-G-A

132571048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526382-G-A

132571048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron variant
orthologous variants: 110526382-G-T

132571178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110526248-C-G

132571471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110525961-T-G

132571486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110525949-G-A

132571486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110525949-G-T

132571552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525874-G-A

132571552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525874-G-C

132571666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525780-G-A

132571666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525780-G-C

132571666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525780-G-T

http://identifiers.org/hco/12/GRCh38#132571672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525774-A-C

132571672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525774-A-G

132571689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525741-C-T

132571716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525715-C-T

132571803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525652-G-T

http://identifiers.org/hco/12/GRCh38#132571804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525651-C-A

132571804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525651-C-G

132571804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525651-C-T

132571807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525648-G-A

132571935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525573-G-A

132571935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525573-G-C

132571935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525573-G-T

http://identifiers.org/hco/12/GRCh38#132571994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525504-C-A

132571994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525504-C-T

132572104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525422-G-A

132572104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525422-G-T

132572137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525399-T-A

132572137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525399-T-C

http://identifiers.org/hco/12/GRCh38#132572138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525398-A-C

132572138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525398-A-T

http://identifiers.org/hco/12/GRCh38#132572214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525346-C-A

132572214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525346-C-T

132572217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525345-G-A

132572217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525345-G-T

132572230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525332-G-A

132572230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525332-G-C

132572230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525332-G-T

132572246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525316-G-A

132572246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525316-G-T

132572268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525291-C-G

132572268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110525291-C-T

132572411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110525176-T-A

132572496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110525105-C-T

http://identifiers.org/hco/12/GRCh38#132572503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110525098-C-A

132572503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110525098-C-T

132572533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110525049-C-T

132572558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110525024-G-T

132572580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110525002-C-T

132572623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 110524959-G-A

132572666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524919-G-A

132572666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524919-G-T

http://identifiers.org/hco/12/GRCh38#132572721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110524884-C-A

132572721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524884-C-T

132572749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524868-T-C

132572758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524860-T-C

132572769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524849-G-A

132572769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524849-G-C

132572769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524849-G-T

132573751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524648-G-A

132573851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524562-C-G

http://identifiers.org/hco/12/GRCh38#132574007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110524420-C-A

132574007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524420-C-T

http://identifiers.org/hco/12/GRCh38#132574019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110524408-C-A

132574105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 110524319-G-T

132574285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524182-G-A

132574285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110524182-G-T

132574388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110524052-C-G

132574388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 110524052-C-T

132574621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523824-G-A

132574621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110523824-G-T

132580823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110520025-G-A

132580826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110520022-G-A

132580877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110519969-G-A

132580877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110519969-G-C

132581036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519854-C-G

132581056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519826-A-G

http://identifiers.org/hco/12/GRCh38#132581154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110519734-C-A

132581154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519734-C-T

132581172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519715-G-A

http://identifiers.org/hco/12/GRCh38#132581207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110519681-C-A

132581207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519681-C-G

132581207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110519681-C-T

132581305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110519621-C-T

132581315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110519611-C-T

132581329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110519597-G-T

132581408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110519518-G-A

132581408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 110519518-G-T

132581707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519271-C-G

132581714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519264-C-G

132581714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519264-C-T

132581721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519253-T-A

http://identifiers.org/hco/12/GRCh38#132581846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110519136-C-A

132581846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110519136-C-T

http://identifiers.org/hco/12/GRCh38#132582044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#110519034-C-A

132582044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519034-C-G

http://identifiers.org/hco/12/GRCh38#132582052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#110519028-C-A

132582052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519028-C-T

132582070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110519010-G-A

132582070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110519010-G-T

132582106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110518974-C-T

http://identifiers.org/hco/12/GRCh38#132583002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110511712-C-A

132583002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511712-C-G

132583002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511712-C-T

132583297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511363-A-G

132583380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511268-G-A

132583380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511268-G-C

132583380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511268-G-T

http://identifiers.org/hco/12/GRCh38#132583608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110511058-C-A

132583608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511058-C-G

132583608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511058-C-T

http://identifiers.org/hco/12/GRCh38#132583612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110511054-C-A

132583612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511054-C-G

132583612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: missense variant
orthologous variants: 110511054-C-T

http://identifiers.org/hco/12/GRCh38#132583622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110511044-C-A

132583622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: synonymous variant
orthologous variants: 110511044-C-G

132583622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: synonymous variant
orthologous variants: 110511044-C-T

http://identifiers.org/hco/12/GRCh38#132583779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510905-C-A

132583779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510905-C-T

http://identifiers.org/hco/12/GRCh38#132583875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510838-C-A

132583875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510838-C-G

132583875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510838-C-T

http://identifiers.org/hco/12/GRCh38#132583892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510828-C-A

132583892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510828-C-T

http://identifiers.org/hco/12/GRCh38#132584079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510647-C-A

132584143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510593-T-A

http://identifiers.org/hco/12/GRCh38#132584201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510542-C-A

132584201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510542-C-T

132584571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510167-G-A

132584585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510149-G-A

132584585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510149-G-T

http://identifiers.org/hco/12/GRCh38#132584625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110510125-A-C

132584625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110510125-A-G

132584825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509934-C-T

132584826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509933-A-G

132584826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509933-A-T

http://identifiers.org/hco/12/GRCh38#132584924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110509881-C-A

132584924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509881-C-T

132584937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509865-T-C

132584937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509865-T-G

http://identifiers.org/hco/12/GRCh38#132584957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110509845-C-A

132584957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509845-C-T

http://identifiers.org/hco/12/GRCh38#132584979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#110509821-C-A

132584979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509821-C-T

132585064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509746-G-A

132585064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29308
most severe consequence: 3 prime UTR variant
orthologous variants: 110509746-G-T