28348751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869874-G-T

http://identifiers.org/hco/3/GRCh38#28348833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117869793-C-A

28348833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117869793-C-T

28348988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869642-G-A

28348988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869642-G-T

http://identifiers.org/hco/3/GRCh38#28349043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#117869587-C-A

28349043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869587-C-T

28349140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117869476-A-G

28349168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869428-G-A

28349168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869428-G-T

28349171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 117869425-G-A

28349215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117869372-A-G

28349300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117869294-T-C

28349316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117869279-T-A

28351449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117868371-T-C

28351743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117867873-A-G

28351758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117867858-T-C

28351889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117867770-G-A

http://identifiers.org/hco/3/GRCh38#28352113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117867602-A-C

28377853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117864949-G-C

28377984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117864572-C-G

28378306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117864242-T-A

28383987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117862677-C-T

http://identifiers.org/hco/3/GRCh38#28384059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117862605-A-C

28386320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117862487-A-G

28386512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117862293-A-G

28386530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117862276-A-G

28386551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117862255-A-G

28387104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117861564-A-G

28396311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117861336-C-T

http://identifiers.org/hco/3/GRCh38#28397298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117860446-A-C

28398007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117859637-C-T

28398043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117859573-G-T

28398162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117859456-T-C

28398309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117859308-T-C

28398330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117859287-A-G

28407664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117858620-A-G

28407687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117858598-G-C

28407687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117858598-G-T

28407773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117858520-A-G

http://identifiers.org/hco/3/GRCh38#28408193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117858130-C-A

28408193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117858130-C-T

28408390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857918-C-G

28408390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857918-C-T

28408491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857785-G-A

http://identifiers.org/hco/3/GRCh38#28408493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117857783-A-C

28408570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857710-A-G

28408590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857691-C-T

28408819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117857050-T-A

http://identifiers.org/hco/3/GRCh38#28412824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117843514-C-A

28412836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843502-T-A

28412950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843397-G-A

28412992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117843363-T-G

28413070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: non_coding_transcript_exon_variant, start_lost
orthologous variants: 117843300-T-C

28413075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843287-A-G

28413075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 117843287-A-T

28413106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843256-G-A

28413106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843256-G-T

28413231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843109-G-C

28413231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843109-G-T

28413272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117843068-T-C

28413283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 117843057-C-G

28413283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843057-C-T

28413322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843018-A-G

28413326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117843014-G-A

28413326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117843014-G-C

http://identifiers.org/hco/3/GRCh38#28424590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117833805-A-C

28424590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833805-A-G

28424614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833782-A-G

28424661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833736-C-G

28424725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833676-C-T

28424726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833675-G-A

http://identifiers.org/hco/3/GRCh38#28424759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117833650-A-C

28424836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117833560-T-C

http://identifiers.org/hco/3/GRCh38#28425032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117832936-A-C

28425051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832911-T-C

28425210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832772-T-G

28425573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832409-C-T

http://identifiers.org/hco/3/GRCh38#28425717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117832264-C-A

28425803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832209-A-G

28431213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832165-C-T

28431216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117832162-A-G

28431713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831434-A-G

28432429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831262-T-C

28432444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831247-G-A

28432529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831166-G-A

28432529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117831166-G-T

28432882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830783-C-G

28433060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830634-G-A

28433176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830494-T-C

28433212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830459-A-T

28433260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830411-C-G

28433261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830410-T-G

28433278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830405-G-T

28434046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117830010-T-C

28434310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829601-T-C

28434322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829589-G-C

28434322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829589-G-T

28434351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829561-A-G

http://identifiers.org/hco/3/GRCh38#28434363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117829549-C-A

28434402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

28434464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117829172-A-G

28434926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828190-T-C

28434936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828179-A-G

28434989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828137-A-G

28434989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828137-A-T

28434991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828135-A-G

28435059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828062-G-A

http://identifiers.org/hco/3/GRCh38#28435064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117828057-C-A

28435064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828057-C-T

http://identifiers.org/hco/3/GRCh38#28435065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117828056-C-A

28435065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117828056-C-T

28435118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117828009-G-T

28435164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117827963-C-G

28435379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827756-G-A

28435379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827756-G-C

28435379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827756-G-T

28435992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827505-T-C

28436211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827351-T-G

http://identifiers.org/hco/3/GRCh38#28436368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117827246-C-A

28436368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827246-C-T

28436746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117827047-A-G

28437547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117825433-C-T

28437667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117825311-T-G

http://identifiers.org/hco/3/GRCh38#28438133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117825089-C-A

28438278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117824951-G-A

28438388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117824834-G-A

28438395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117824827-C-G

28452711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117819521-A-G

28453198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117819162-A-T

28453260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117819106-A-G

28453367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117819023-G-C

28453578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818968-A-G

28453782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818783-A-T

http://identifiers.org/hco/3/GRCh38#28457151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117818674-A-C

http://identifiers.org/hco/3/GRCh38#28457230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117818616-A-C

28457248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818598-A-G

http://identifiers.org/hco/3/GRCh38#28457295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117818555-A-C

28457437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818417-T-A

28457577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818276-C-G

28457577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117818276-C-T

28458141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117807429-A-G

28458202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117807380-C-T

http://identifiers.org/hco/3/GRCh38#28458338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117807253-A-C

28458365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117807226-G-A

28458501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117807087-A-G

28458547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117807041-C-T

28458649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806941-A-G

28458652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806938-G-A

28458652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806938-G-T

28458751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806849-G-A

28458854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806756-T-G

28459259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117806536-A-G

28460186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805767-G-C

28460186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805767-G-T

28460478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805526-A-T

28460517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805496-G-T

28460650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805371-C-G

http://identifiers.org/hco/3/GRCh38#28460852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117805181-A-C

28460903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805131-A-G

28460944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805094-G-A

28460944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805094-G-T

28460947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117805091-A-G

http://identifiers.org/hco/3/GRCh38#28460994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117805048-C-A

28460994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 117805048-C-T

http://identifiers.org/hco/3/GRCh38#28461005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117805037-A-C

28461005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117805037-A-G

28461051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117804983-T-C

28461064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117804969-T-C

28461085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117804948-T-C

28461099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117804934-A-G

28461105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117804910-G-T

28461655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117804159-A-G

28461731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117804087-T-C

http://identifiers.org/hco/3/GRCh38#28461816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117804016-C-A

28461832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117804004-G-A

http://identifiers.org/hco/3/GRCh38#28461854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117803982-A-C

http://identifiers.org/hco/3/GRCh38#28461861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117803969-A-C

28461881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803947-G-A

28461886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803942-G-T

28461940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803912-T-C

28462122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803715-G-T

28462138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803699-G-A

28462151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803687-C-T

28462220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803646-A-G

28462755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803185-T-G

28462767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803176-G-A

28462899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117803041-A-G

28462970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117802975-C-T

28463032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117802901-G-C

28463106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117802829-T-C

28463126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117802809-T-G

28463183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117802763-A-G

28465284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117798056-C-T

28465315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117798024-C-T

http://identifiers.org/hco/3/GRCh38#28465635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117797738-A-C

28475404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117796937-G-T

28475556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117796661-C-T

http://identifiers.org/hco/3/GRCh38#28475619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117796600-C-A

28476181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117796098-A-G

28476231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117796048-C-G

28476257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117796023-C-G

28477340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794846-C-T

28477361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794829-C-G

28477823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794394-C-G

28478012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794254-C-T

28478120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794149-T-C

28478120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794149-T-G

28478176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117794092-G-T

28478344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117794012-A-G

28478344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117794012-A-T

28478420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793998-T-C

http://identifiers.org/hco/3/GRCh38#28478456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117793961-C-A

28478456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793961-C-T

28478495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793923-A-G

28478669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793801-A-G

28478704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793767-T-A

28478704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793767-T-C

28478704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793767-T-G

28478747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793731-A-T

28478752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793712-G-T

http://identifiers.org/hco/3/GRCh38#28478826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117793632-A-C

28478826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117793632-A-G

28478903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 117793555-G-A

28478910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 117793548-T-C

28478943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793520-T-A

28478943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793520-T-C

28478985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793479-T-C

http://identifiers.org/hco/3/GRCh38#28479005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117793464-C-A

28479005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793464-C-T

28479049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117793421-A-G

http://identifiers.org/hco/3/GRCh38#28491174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117790171-C-A

28491626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117789555-G-T

http://identifiers.org/hco/3/GRCh38#28491674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117789506-A-C

28491756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117789424-T-G

28491787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117789397-T-A

28492061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117789145-T-C

28492069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117789137-T-C

http://identifiers.org/hco/3/GRCh38#28492204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117788876-C-A

28492204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788876-C-T

28492370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788703-A-G

28492386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788697-T-C

28492493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788591-C-T

28492611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788479-G-T

28492751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117788346-T-G

28503468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117786843-C-T

http://identifiers.org/hco/3/GRCh38#28503532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117786795-A-C

28503532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117786795-A-G

28504388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117786304-A-G

http://identifiers.org/hco/3/GRCh38#28504800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117785888-A-C

28505095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117785624-C-T

28505489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117785255-C-T

28513103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777864-G-A

28513177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777792-G-A

28513199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777770-T-A

28513392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777523-T-C

28513702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777274-T-A

28513920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777080-T-C

http://identifiers.org/hco/3/GRCh38#28514009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117777023-C-A

28514019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777013-T-A

28514019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117777013-T-C

28514072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117776962-T-C

28514072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117776962-T-G

http://identifiers.org/hco/3/GRCh38#28514100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117776934-C-A

28514100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117776934-C-T

28514182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117776850-T-C

28514819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117775682-G-A

28514833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117775661-T-A

28514998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117775316-C-G

28515419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117774905-T-A

28515419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117774905-T-G

28515474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117774825-A-T

28515499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117774800-T-G

28516659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117773395-T-A

28518779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117763128-C-T

http://identifiers.org/hco/3/GRCh38#28518879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117763031-A-C

28518893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117763012-A-G

28518914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762798-G-C

28518918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762794-G-C

28518989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762617-C-T

28518996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762610-T-C

28519371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762280-T-G

28519443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117762210-G-A

28519933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117761799-C-G

28520763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117760931-C-T

28520860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117760836-A-G

28521188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117758103-T-C

28521569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757284-C-T

28521800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117757053-A-G

28522568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756436-T-A

28522625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756378-A-G

28522652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756351-G-A

28522652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756351-G-T

28522732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756284-G-T

28522744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117756275-T-C

28523080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117755793-T-C

28523321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117755593-A-G

28523609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117755292-A-T

28524514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117753553-G-A

28524709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117753352-T-A

28524942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117753133-T-C

28524949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117753126-T-C

28524959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117753116-A-G

http://identifiers.org/hco/3/GRCh38#28525110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117752971-C-A

28525305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 117752783-G-A

28532614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117749458-T-C

28532845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117749246-T-C

28532862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117749230-A-G

28533033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117749097-G-A

28533058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117749072-G-A

28533474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747665-G-A

28533763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747385-A-G

28533794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747355-G-C

28533794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747355-G-T

28533842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747310-G-A

28533848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117747304-C-T

28534138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117746702-C-T

28534362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117746434-G-C

http://identifiers.org/hco/3/GRCh38#28534618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117746218-A-C

28534800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117746045-T-C

28535011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: intron variant
orthologous variants: 117745845-C-T

28538009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3 prime UTR variant
orthologous variants: 117744499-C-T

28538053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3 prime UTR variant
orthologous variants: 117744464-G-A

http://identifiers.org/hco/3/GRCh38#28538118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#117744402-C-A

28538118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23574
most severe consequence: 3 prime UTR variant
orthologous variants: 117744402-C-T