59171590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12479572-A-G

59171679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 12479478-G-C

59171728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12479389-G-C

59172438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478728-G-A

59172438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478728-G-T

59172466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12478700-C-T

59172481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12478685-G-A

59172481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12478685-G-C

59172481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12478685-G-T

59172543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478623-G-A

59172543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478623-G-T

http://identifiers.org/hco/11/GRCh38#59172555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12478620-C-A

59172555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478620-C-G

59172555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12478620-C-T

59172919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12478282-A-G

59173368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 12477818-C-G

59173792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12477353-G-C

59173793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12477352-G-A

59173837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12477294-C-T

59173971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12477154-G-A

59173972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12477153-G-A

59174138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12476974-C-T

59174185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12476928-G-C

http://identifiers.org/hco/11/GRCh38#59174334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#12476761-A-C

59174409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12476686-T-A

59174409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12476686-T-G

http://identifiers.org/hco/11/GRCh38#59174476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#12476642-C-A

59174476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12476642-C-T

http://identifiers.org/hco/11/GRCh38#59174686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12476419-C-A

59174807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12476135-G-T

59174886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12476035-T-A

59175095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475828-T-C

59175100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475823-C-T

59175149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475770-G-T

59175602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475329-G-A

59175637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475294-G-A

59175637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475294-G-C

59175637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475294-G-T

59175915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475203-A-T

59176066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12475058-A-G

59176411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474765-G-A

http://identifiers.org/hco/11/GRCh38#59176515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12474671-A-C

59176515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474671-A-G

59176700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474503-G-A

59176853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474347-A-G

59176862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12474310-C-G

59177331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12473709-C-T

59177454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12473598-C-G

http://identifiers.org/hco/11/GRCh38#59177575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12473478-A-C

59177784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12473346-G-A

59177876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12473282-T-C

59177956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12473201-T-G

59177978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12473179-T-G

59178013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12473143-G-A

59178019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12473137-T-G

59178197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472973-A-G

59178220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472948-G-A

59178272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472900-T-A

59178272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472900-T-G

59178282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472891-T-G

59178632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472568-C-T

59178903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472304-G-A

59178963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472244-A-G

59178991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472217-T-A

59179200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12472011-T-G

59180272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12471460-T-C

59181279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470327-A-G

59181438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470178-G-A

59181438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470178-G-C

59181459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470159-G-A

59181557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470070-T-C

59181631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12470000-G-T

59181795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469856-G-A

59182020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469631-A-G

59182267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469393-G-A

59182267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469393-G-C

59182267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469393-G-T

59182278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469382-A-G

59182311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469349-G-A

59182385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12469275-G-T

59182401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12469259-T-C

59182508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12469159-A-G

http://identifiers.org/hco/11/GRCh38#59182568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12469080-C-A

59183124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468790-T-C

http://identifiers.org/hco/11/GRCh38#59183241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12468733-A-C

59183450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468615-C-T

59183876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468166-T-C

59184019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468045-A-G

59184069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12468011-C-T

59184102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467978-C-T

59184129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467955-G-A

59184147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467937-C-T

59184171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467913-G-A

59184321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467781-G-A

59184509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467604-C-T

59184589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467517-G-C

59184685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12467421-C-T

59185217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466928-A-T

http://identifiers.org/hco/11/GRCh38#59185358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12466787-C-A

59185358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466787-C-T

59185438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466629-G-A

59185438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466629-G-T

59185673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466393-C-T

59186042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12466016-C-G

59186260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465800-G-C

59186469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12465608-G-C

59186486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12465591-C-T

59187223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465065-G-C

59187243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465045-T-C

59187262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12465026-G-A

59187647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12464667-T-A

59187720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12464586-C-T

59187762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12464538-G-A

59188231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12464289-G-A

59188344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12464244-G-A

59188430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12464161-G-C

59188655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463931-T-C

59188655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463931-T-G

59188678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463908-T-C

59188678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463908-T-G

http://identifiers.org/hco/11/GRCh38#59188693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12463893-C-A

59188836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463748-A-G

http://identifiers.org/hco/11/GRCh38#59188849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12463735-A-C

59188869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12463715-T-A

59189081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462866-G-A

59189081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462866-G-T

59189212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12462737-A-G

59189343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462605-T-G

59189344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462604-G-A

59189344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462604-G-T

59189355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462593-A-T

http://identifiers.org/hco/11/GRCh38#59189361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12462587-A-C

59189361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462587-A-G

59189362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462586-G-A

http://identifiers.org/hco/11/GRCh38#59189410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12462542-C-A

59189410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462542-C-T

59189439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462513-T-C

59189439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462513-T-G

59189466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462485-A-T

59189475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462476-G-A

59189488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12462463-C-T

59189871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12462139-G-A

59190126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461868-C-T

59190339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461660-T-C

59190516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12461469-C-T

http://identifiers.org/hco/11/GRCh38#59190964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12460990-C-A

59190965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460989-A-G

59191107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12460476-T-A

59191107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12460476-T-C

59191180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460403-G-A

59191180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460403-G-C

59191180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460403-G-T

59191210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460372-T-A

59191210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460372-T-C

59191227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460356-T-C

59191403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460193-T-C

59191444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460153-T-A

59191465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460132-A-G

59191466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12460131-A-G

59191667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459933-A-G

59191866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459804-G-A

59191889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459781-G-A

http://identifiers.org/hco/11/GRCh38#59191899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12459771-A-C

59191983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459666-G-A

59191983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459666-G-T

http://identifiers.org/hco/11/GRCh38#59191997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12459652-A-C

59191997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12459652-A-G

59192227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12459459-G-A

59192378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12459087-G-A

59192378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12459087-G-T

59192650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12458738-G-A

59192713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12458673-T-C

59192938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12458479-T-A

59193301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457775-A-G

59193448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457640-G-A

59193448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457640-G-C

59193448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457640-G-T

59193450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457638-T-C

59193564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457532-C-T

59193664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457434-T-C

59193811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457294-C-T

59193841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457264-G-A

59193841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457264-G-C

59193841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457264-G-T

59193876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457224-C-T

59193965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457135-T-C

59193965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457135-T-G

http://identifiers.org/hco/11/GRCh38#59193967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12457133-C-A

59193967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457133-C-T

59193968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457132-G-A

59193994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457102-T-C

59193998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457098-G-A

59193998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457098-G-T

59194034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12457042-C-T

59194582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456194-C-G

59194582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456194-C-T

59194592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456186-C-G

59194592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456186-C-T

59194744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456058-A-G

59194762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456040-G-C

59194762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456040-G-T

59194827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456014-T-G

59194830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12456011-T-C

59194865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron variant
orthologous variants: 12455976-G-A

59194908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12455936-A-G

59194994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12455852-G-A

59194994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12455852-G-T

59195046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12455801-T-C

59195048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12455799-G-T

http://identifiers.org/hco/11/GRCh38#59195077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455779-C-A

http://identifiers.org/hco/11/GRCh38#59195185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455672-C-A

http://identifiers.org/hco/11/GRCh38#59195319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455538-C-A

http://identifiers.org/hco/11/GRCh38#59195358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455499-C-A

59195358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12455499-C-G

59195358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12455499-C-T

http://identifiers.org/hco/11/GRCh38#59195375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455482-C-A

59195376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12455481-C-G

59195377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12455480-T-C

59195380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455477-C-G

59195449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455423-T-A

59195449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455423-T-C

http://identifiers.org/hco/11/GRCh38#59195504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455389-C-A

59195504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455389-C-T

http://identifiers.org/hco/11/GRCh38#59195519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12455376-C-A

59195519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455376-C-T

59195625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12455277-C-T

59195927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454986-G-A

59196315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454604-G-A

http://identifiers.org/hco/11/GRCh38#59196357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12454565-A-C

59197301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12454045-T-A

59197425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453925-G-A

59197627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453743-G-A

59197627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453743-G-C

http://identifiers.org/hco/11/GRCh38#59197793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12453606-A-C

59197833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12453567-G-A

59198176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452962-G-A

59198211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452927-A-G

59198221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452913-A-G

59198373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452768-G-A

59198659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452416-C-T

59198691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12452377-G-T

59198985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451347-G-A

59199125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451208-A-G

59199265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451065-T-C

59199290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12451040-T-C

http://identifiers.org/hco/11/GRCh38#59199535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12450832-C-A

http://identifiers.org/hco/11/GRCh38#59199623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12450738-C-A

59199623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450738-C-T

59199654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450709-G-A

59199654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450709-G-T

59199756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12450609-A-T

59199886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12450514-T-C

59200392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449882-A-G

59200534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12449737-A-G

59201231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449160-C-T

http://identifiers.org/hco/11/GRCh38#59201337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12449059-C-A

59201345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12449051-G-A

59201904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448158-T-G

59201920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448142-C-T

59202046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448044-C-T

59202049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12448041-G-C

http://identifiers.org/hco/11/GRCh38#59204508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12447234-C-A

59204508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447234-C-T

59204545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447200-T-C

59204562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447183-G-T

http://identifiers.org/hco/11/GRCh38#59204615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12447132-A-C

59204615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447132-A-G

59204628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447119-G-C

59204628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12447119-G-T

59204784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: missense variant
orthologous variants: 12446963-A-G

59204910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446837-G-C

59204910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446837-G-T

59204936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446829-G-A

59204936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446829-G-T

59205043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446736-C-T

59205066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446713-G-A

59205211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446572-G-T

59205464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446320-T-C

59205559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446256-C-T

http://identifiers.org/hco/11/GRCh38#59205688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12446126-C-A

59205792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446033-G-A

59205792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12446033-G-T

59205857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445972-T-C

59205891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445937-C-T

59205995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445837-C-T

59206007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445825-T-C

http://identifiers.org/hco/11/GRCh38#59206024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12445808-C-A

59206024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445808-C-T

59206057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445775-G-A

59206057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445775-G-T

59206060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445772-C-T

59206066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445766-T-A

59206066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445766-T-C

59206192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445628-A-G

59206206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445612-T-C

59206211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445607-G-C

http://identifiers.org/hco/11/GRCh38#59206234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12445581-A-C

59206234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445581-A-G

59206242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445573-A-G

59206286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445529-A-G

59206377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445443-A-G

59206391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445429-G-A

59206391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445429-G-C

59206391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445429-G-T

http://identifiers.org/hco/11/GRCh38#59206406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12445415-C-A

59206406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445415-C-T

59206420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445401-T-C

59206683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445131-A-G

59206738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445092-C-T

59206828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445010-A-G

59206828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12445010-A-T

59206966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444876-C-T

59206995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444847-G-A

59207068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444769-G-A

59207068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444769-G-T

59207238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444608-C-G

59207260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444591-A-T

59207272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444580-G-T

59207476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444385-T-C

59207559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444307-A-G

59207572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444294-C-T

59207576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444290-C-G

http://identifiers.org/hco/11/GRCh38#59207584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12444282-C-A

http://identifiers.org/hco/11/GRCh38#59207668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#12444209-C-A

59207668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444209-C-T

59207669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444208-T-C

59207675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12444202-A-T

59207977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443897-T-C

http://identifiers.org/hco/11/GRCh38#59207991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#12443876-C-A

59207991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443876-C-G

59208074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3 prime UTR variant
orthologous variants: 12443790-T-C

59208136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443729-T-C

59208231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443632-G-T

http://identifiers.org/hco/11/GRCh38#59208293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#12443570-C-A

59208294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443569-C-T

59208351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443514-T-A

59208351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443514-T-G

59208377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443484-A-G

59208442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12443418-A-T

59208505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29151
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 12442935-G-T