http://identifiers.org/hco/10/GRCh38#113854683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#56536953-C-A

113854683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 56536953-C-T

113854736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 56537005-T-C

113854832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56537079-T-C

113854845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 56537092-G-A

http://identifiers.org/hco/10/GRCh38#113854935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56537177-A-C

113854935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56537177-A-G

113854935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56537177-A-T

113854968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 56537210-G-A

113854968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 56537210-G-T

http://identifiers.org/hco/10/GRCh38#113855077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56537319-C-A

113855077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56537319-C-T

113856234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 56537918-T-C

113856413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538096-A-G

113856440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538117-T-G

113856579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538254-A-G

113856920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538544-A-G

113857032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538665-A-G

113857217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538862-C-G

113857305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538935-A-G

113857331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56538969-G-A

113857630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539216-A-G

113858096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539776-C-T

113858247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56539906-A-G

113858397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540043-T-C

113858410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540058-T-G

113858458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540111-T-G

113858467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540120-A-G

113858467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56540120-A-T

http://identifiers.org/hco/10/GRCh38#113858721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56540378-A-C

113858721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540378-A-G

113858729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540386-T-A

113858729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540386-T-C

113858736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540393-G-A

113858736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540393-G-C

113858786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540441-G-A

113858786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540441-G-T

113858902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540627-T-G

http://identifiers.org/hco/10/GRCh38#113858930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56540655-C-A

113858930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540655-C-G

113858930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56540655-C-T

113859505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56541204-T-C

http://identifiers.org/hco/10/GRCh38#113859652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56541325-A-C

113859686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56541358-A-T

113859846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56541564-A-G

113859846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56541564-A-T

113859948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56541663-T-G

113860058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56541749-C-G

113860120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542175-G-C

113860169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542237-T-C

113860541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542623-G-A

113860565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542635-A-G

113861086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56542849-G-A

113861250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543011-A-G

113861268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543029-T-G

113861827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56543518-T-A

113865838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56545956-A-G

113865846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56545964-A-G

113865914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546013-C-T

113865979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546070-A-G

113866306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546343-A-G

http://identifiers.org/hco/10/GRCh38#113866315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56546350-A-C

http://identifiers.org/hco/10/GRCh38#113866555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56546748-A-C

113866594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546788-A-G

113866626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546822-C-G

113866686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56546880-G-T

113866995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56547148-T-C

113866995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56547148-T-G

113867332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56547483-A-G

113867587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 56547718-C-T

113868337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548848-C-G

113868337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 56548848-C-T

http://identifiers.org/hco/10/GRCh38#113868434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56548939-C-A

113871361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56553132-G-A

113871949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56554031-T-C

113872648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56554920-A-T

113872694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56554972-A-G

113872756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555040-T-A

113872756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555040-T-G

113873045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555324-C-T

113873052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555344-T-A

113873096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555387-C-T

113873298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555563-C-G

113873308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555576-T-A

113873344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56555611-C-T

113874646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56556590-C-T

http://identifiers.org/hco/10/GRCh38#113874650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56556594-A-C

113874650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56556594-A-G

113875132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56557131-C-T

113876364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56558711-G-A

113876441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56558777-G-A

113876441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56558777-G-T

113876504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56558832-T-C

113876669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56558996-C-T

113876693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56559020-T-C

113876756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56559083-A-G

113877056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56559392-G-A

113877056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56559392-G-C

113877829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56560102-T-C

113877877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56560147-G-A

113877877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56560147-G-T

113878169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561367-A-T

113878308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561528-T-A

113878328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561548-G-T

113878562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561774-C-G

113878562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561774-C-T

113878584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561796-G-A

113878772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56561935-G-C

113879042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56562175-T-C

113879090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56562213-A-G

113879143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56562272-C-T

113879151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56562280-C-T

113880378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56563634-A-T

113880636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56563852-G-A

113880678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56563880-T-C

113880750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56563933-T-G

http://identifiers.org/hco/10/GRCh38#113884103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56564470-C-A

113884103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564470-C-G

113884137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564492-T-C

113884137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564492-T-G

113884238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564574-T-A

113884286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56564622-T-G

http://identifiers.org/hco/10/GRCh38#113884325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56564661-A-C

113884325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56564661-A-G

113884366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56564702-T-C

113884366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56564702-T-G

113884384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564720-T-C

113884407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564963-A-G

113884412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564968-T-A

113884428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564984-T-A

113884428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56564984-T-C

113884479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56565022-T-C

113884480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56565023-T-C

113884831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56565327-G-A

113885108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56565593-C-T

113888729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56568979-G-C

113889363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56569502-C-T

113897305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56574388-T-C

113897412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56574488-C-T

113897682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56574734-G-C

113897682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56574734-G-T

113897971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56576495-T-C

113898003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56576505-G-T

113898305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56576764-T-C

113898359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56576798-A-G

113898534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56576968-C-T

http://identifiers.org/hco/10/GRCh38#113898582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56577016-A-C

113898653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577087-G-A

113898690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577131-A-G

113898812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577213-C-T

113899127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577385-C-T

113899206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577468-C-G

113899206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577468-C-T

113899243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56577502-T-C

113900276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56578795-C-G

113900396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56578903-G-C

113900638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579117-A-G

113900808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579212-A-G

113900847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579250-T-C

113900893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579281-T-A

113901270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579652-A-G

http://identifiers.org/hco/10/GRCh38#113901392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56579769-A-C

113901392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56579769-A-G

113901840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56580182-C-T

113901846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56580188-A-G

113901873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56580215-C-G

113901873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56580215-C-T

http://identifiers.org/hco/10/GRCh38#113901924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56580258-C-A

113901924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580258-C-T

113902039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580344-G-A

113902305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580676-T-G

http://identifiers.org/hco/10/GRCh38#113902329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56580688-C-A

113902329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580688-C-T

113902678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580984-G-A

113902678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56580984-G-T

113902702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56581021-T-G

113903201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56581804-G-A

113903257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56581845-G-A

113903388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56581969-G-T

113903596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56582158-A-T

http://identifiers.org/hco/10/GRCh38#113903613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56582175-A-C

113903766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582323-A-G

113903811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582354-G-A

113903811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582354-G-T

http://identifiers.org/hco/10/GRCh38#113903813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56582356-C-A

113903813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582356-C-T

113904116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582648-G-T

113904310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582829-A-G

113904340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56582858-C-T

113904842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56583257-C-T

113904907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56583322-C-G

113904907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56583322-C-T

113904915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56583330-T-C

http://identifiers.org/hco/10/GRCh38#113904991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56583406-A-C

http://identifiers.org/hco/10/GRCh38#113905050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56583465-C-A

113905050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56583465-C-T

113905175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56583584-A-G

113905175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56583584-A-T

http://identifiers.org/hco/10/GRCh38#113906120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56584513-C-A

113906212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56584560-C-T

113906312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56584659-T-G

113906335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: intron variant
orthologous variants: 56584681-G-A

113907890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 56585027-A-T

113908293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56585701-A-G

113908338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56585746-T-G

113908341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: synonymous variant
orthologous variants: 56585749-A-G

http://identifiers.org/hco/10/GRCh38#113908402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56585810-A-C

113908402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56585810-A-T

113908528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: missense variant
orthologous variants: 56585936-G-A

http://identifiers.org/hco/10/GRCh38#113908616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56586012-C-A

113908616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586012-C-T

113908710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586085-A-T

113908752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586128-T-A

113908766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586141-A-G

113909324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586655-G-T

113909453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586791-G-T

113909633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586948-A-T

113909635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586950-T-G

113909654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56586967-T-C

113909756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56587095-T-G

113909803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56587138-A-G

http://identifiers.org/hco/10/GRCh38#113910546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56587500-C-A

113910552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56587506-T-C

http://identifiers.org/hco/10/GRCh38#113911756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56588232-A-C

113911804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588276-G-T

113912002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588440-T-A

113912209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588636-T-C

113912212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588639-A-G

113912212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588639-A-T

113912214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588641-G-A

113912274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588704-T-C

113912466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588902-G-A

113912519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56588954-G-T

http://identifiers.org/hco/10/GRCh38#113912600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56589023-C-A

113912617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589040-A-G

113912716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589124-G-T

113912877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589241-C-T

113912878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589242-G-A

113912878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589242-G-C

113912878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589242-G-T

113912902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589256-G-T

113913005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589312-A-G

113913599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589788-A-G

113913639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56589820-A-G

113914570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590037-T-C

http://identifiers.org/hco/10/GRCh38#113914908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56590331-C-A

113914908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590331-C-T

113915024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590440-T-C

113915131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590538-C-T

http://identifiers.org/hco/10/GRCh38#113915166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#56590584-C-A

113915214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590626-A-G

113915218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56590630-G-A

113916241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591109-A-T

113916411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591273-T-G

113916472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591333-T-A

113916472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591333-T-C

113916472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591333-T-G

113916612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591447-A-G

113916646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591479-G-C

113916687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591512-T-G

113916750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591561-A-G

113917082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591829-A-G

113917104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24731
most severe consequence: 3 prime UTR variant
orthologous variants: 56591848-G-A