113532712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44153201-G-A

113532712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44153201-G-T

http://identifiers.org/hco/3/GRCh38#113532982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44152942-C-A

113532982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44152942-C-G

113532982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44152942-C-T

113532991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44152933-T-A

113532991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44152933-T-C

http://identifiers.org/hco/3/GRCh38#113533115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44152796-C-A

113533115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152796-C-T

113533127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152784-C-T

113533157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152754-G-A

113533157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152754-G-T

113533178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152733-A-G

113533182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152729-G-A

113533182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152729-G-C

113533190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44152721-A-G

http://identifiers.org/hco/3/GRCh38#113533273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44152631-C-A

113533290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152614-T-C

http://identifiers.org/hco/3/GRCh38#113533302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44152602-C-A

113533302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152602-C-G

113533302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152602-C-T

113533309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152595-T-C

113533314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152590-G-A

113533314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152590-G-C

113533314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152590-G-T

113533538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152367-C-G

113533543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152363-A-G

113533789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44152203-C-T

113534231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151850-A-G

113534250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151829-T-G

113534454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151664-C-T

113534522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151600-C-T

113534529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151593-A-G

113534634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44151490-G-T

http://identifiers.org/hco/3/GRCh38#113534686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44151438-A-C

113534756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44151405-G-A

113535961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44150067-C-G

113536006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44150024-G-A

http://identifiers.org/hco/3/GRCh38#113536078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44149955-C-A

113536078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44149955-C-G

113536217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44149809-C-T

113536753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44149301-A-T

113536986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44149075-T-G

113537559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144502-T-C

113537559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144502-T-G

113537692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144390-C-T

113538098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144292-T-A

http://identifiers.org/hco/3/GRCh38#113538146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44144252-C-A

113538195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144204-G-A

113538195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144204-G-C

113538343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44144050-G-C

113538637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143786-C-T

113538709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143603-G-A

113538709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143603-G-C

113538818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143510-G-A

113538818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143510-G-T

113538846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143483-A-T

113539039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143444-A-G

113539133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143354-C-T

113539237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44143275-C-T

113545986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44141347-T-C

113546513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44140710-A-G

113546656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44140575-T-C

http://identifiers.org/hco/3/GRCh38#113546776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44140469-C-A

113547004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44140262-A-G

113547563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44138841-T-C

113547652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44138755-G-A

113548029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44138423-G-A

113548834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44131404-T-G

113548950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44131512-A-G

113548950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44131512-A-T

http://identifiers.org/hco/3/GRCh38#113548964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44131526-C-A

http://identifiers.org/hco/3/GRCh38#113548970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44131532-C-A

113549107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44131649-T-C

113549443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132143-T-C

113549537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132227-C-T

113549609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132308-T-C

113549609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132308-T-G

113549718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132436-A-G

113549719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44132437-T-A

113550501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133127-A-G

113550507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133133-G-A

113551412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133542-T-C

113551503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133629-G-A

http://identifiers.org/hco/3/GRCh38#113551659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44133796-C-A

113551659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133796-C-T

113551762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44133903-A-G

113551952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44134015-G-A

113552070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44134132-T-G

113552210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44134253-C-T

113552238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44134281-G-A

113552250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44134293-T-C

113552616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44134970-G-A

113552654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135005-T-C

113552693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135044-C-T

113552798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135135-C-T

113553138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135449-A-G

113553379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135703-C-T

113553488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135828-A-G

113553656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44135981-A-G

113554981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44136467-G-C

113555041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44136527-C-T

113555269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44136740-C-T

113555287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44136758-C-T

113555749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137191-T-G

113555868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137286-G-A

113555868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137286-G-C

113555868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137286-G-T

113555877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137289-G-T

113555900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137312-C-T

113555995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137429-G-A

113556131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137569-C-T

http://identifiers.org/hco/3/GRCh38#113556263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44137755-A-C

113556264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137756-A-G

113556463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44137937-C-T

113558620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130243-C-T

113558626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130237-A-G

113558726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130150-A-G

113558742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130134-C-T

113558777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130102-G-A

113558777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130102-G-T

113558839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130039-T-A

113558842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44130036-T-C

113558895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129983-C-T

113559208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129682-A-G

113559210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129680-G-A

113559281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129629-T-C

113559309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129601-T-C

113559408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44129502-C-T

113560371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44126388-A-G

113560416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44126343-G-A

113560511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44126273-G-A

113560630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44126158-C-T

113561010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44125806-A-G

113561123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44125687-A-G

113561690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44125078-G-T

113562414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44124229-T-A

113562479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44124167-A-G

113562518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44124127-A-G

113562532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44124113-A-G

113564387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44123294-T-G

113564466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44123223-G-A

113564511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44123148-G-A

113564580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44123061-A-T

http://identifiers.org/hco/3/GRCh38#113564707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44122916-A-C

113564725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44122898-G-A

113564976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44122644-C-G

113564996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44122624-T-A

113564996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44122624-T-G

113564999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44122621-A-G

http://identifiers.org/hco/3/GRCh38#113565100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44122564-A-C

113565869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121819-C-G

113566268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121468-A-T

113566277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121460-T-C

113566553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121291-T-C

113566553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121291-T-G

113566640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44121164-A-G

113566871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120957-T-C

113567045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120790-C-T

113567053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120782-A-G

113567204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120651-G-A

113567449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120417-A-G

113567495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44120371-T-C

113567583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44120290-T-C

113567643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44120230-G-A

http://identifiers.org/hco/3/GRCh38#113567733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44120134-A-C

113567733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44120134-A-G

113570579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44119855-C-G

113570595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44119837-A-G

113570737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44119718-G-C

113570803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44119673-G-A

http://identifiers.org/hco/3/GRCh38#113571133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44119365-C-A

113571164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44119334-G-A

113574208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44115063-T-C

113574341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44114937-G-C

113574557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44114743-T-C

113575010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44114351-A-G

http://identifiers.org/hco/3/GRCh38#113575057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44114314-A-C

113575624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112846-G-A

113575624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112846-G-C

113575636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112834-G-A

113575739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112734-T-C

http://identifiers.org/hco/3/GRCh38#113575831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44112648-A-C

113576146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112359-T-A

113576404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112122-A-G

113576456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44112069-T-C

113576758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111794-G-A

http://identifiers.org/hco/3/GRCh38#113576777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44111781-C-A

113576777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111781-C-T

http://identifiers.org/hco/3/GRCh38#113576780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44111778-A-C

http://identifiers.org/hco/3/GRCh38#113576795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44111765-C-A

113576795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111765-C-T

http://identifiers.org/hco/3/GRCh38#113576798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44111762-C-A

113576875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111688-T-C

113576981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111598-T-C

113576999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111580-T-C

113577075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111508-A-G

113577136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111469-G-A

113577359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44111257-G-T

113579407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44109097-G-T

113579408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44109096-G-A

113579547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44108996-G-T

113580019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44108303-A-T

113580451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107895-C-T

113580538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107812-T-A

113580570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107780-G-T

http://identifiers.org/hco/3/GRCh38#113580587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44107726-C-A

113580587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107726-C-T

113580598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107715-T-C

113580632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44107681-G-A

113580674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44107639-T-C

113580726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107584-T-C

http://identifiers.org/hco/3/GRCh38#113580771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44107539-A-C

113580850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107464-T-A

http://identifiers.org/hco/3/GRCh38#113580990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44107342-C-A

113580990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107342-C-T

113581035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107297-T-G

113581059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107273-T-C

113581067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107265-G-A

113581087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107245-G-A

113581100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107232-T-A

113581100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107232-T-C

http://identifiers.org/hco/3/GRCh38#113581171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44107127-A-C

113581171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44107127-A-G

113581215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106905-T-C

113581232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106888-C-G

113581232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106888-C-T

http://identifiers.org/hco/3/GRCh38#113581532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44106600-C-A

113581532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44106600-C-T

113581548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44106584-A-G

113581899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106508-A-G

113581904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106503-T-C

113581904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106503-T-G

113581915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106492-G-A

113581915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106492-G-C

113581915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106492-G-T

113581930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106474-T-C

113581930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106474-T-G

http://identifiers.org/hco/3/GRCh38#113581948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44106458-C-A

113581948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106458-C-T

http://identifiers.org/hco/3/GRCh38#113581996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44106417-C-A

http://identifiers.org/hco/3/GRCh38#113581997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44106416-C-A

113582018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106395-T-C

113582018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106395-T-G

113582035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106377-G-A

113582035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106377-G-T

113582207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106199-T-A

113582301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44106091-T-G

113582962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44105220-C-T

http://identifiers.org/hco/3/GRCh38#113583292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44104774-C-A

113583292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104774-C-G

113583292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104774-C-T

http://identifiers.org/hco/3/GRCh38#113583293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44104773-A-C

113583293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104773-A-G

113583309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104757-T-A

http://identifiers.org/hco/3/GRCh38#113583351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44104720-C-A

http://identifiers.org/hco/3/GRCh38#113583380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44104689-C-A

113583380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44104689-C-G

113583506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104563-A-G

113583555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104536-G-A

113583555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104536-G-T

113583598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104496-G-A

113583598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104496-G-C

113583598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44104496-G-T

http://identifiers.org/hco/3/GRCh38#113583668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44104430-A-C

113584096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44103532-C-T

113584537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44103109-A-G

http://identifiers.org/hco/3/GRCh38#113584618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44103041-C-A

113584749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44102835-C-G

113584749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44102835-C-T

113584863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102721-G-T

113584913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102635-G-A

113585007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102423-C-G

http://identifiers.org/hco/3/GRCh38#113585097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44102328-C-A

113585097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102328-C-T

113585121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102304-T-C

113585167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44102259-C-G

113585221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44102205-C-T

113585245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44102181-C-T

113585515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101963-A-T

113585584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101907-T-C

113585665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101809-A-G

113585709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101765-C-G

113585709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101765-C-T

113585946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101557-A-G

113585946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101557-A-T

113585947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101556-C-T

113586005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101492-C-T

113586006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101491-A-G

http://identifiers.org/hco/3/GRCh38#113586024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44101470-C-A

113586149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44101339-C-T

113586457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44100842-G-A

113587648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44098760-A-G

113587661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44098747-T-G

113587729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44098661-G-T

113587922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44098101-A-G

113587934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44098088-G-C

113588103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097962-G-T

113588226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097850-A-G

113588438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097648-G-T

113588634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097471-G-A

113588634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097471-G-C

113588634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097471-G-T

113588641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097464-A-G

113588641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097464-A-T

113588804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44097308-T-A

http://identifiers.org/hco/3/GRCh38#113588806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44097289-C-A

113588806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 44097289-C-T

113588812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44097283-T-A

http://identifiers.org/hco/3/GRCh38#113588846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44097249-C-A

113588941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097034-A-G

113588974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44097003-T-C

113589294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44096745-T-A

http://identifiers.org/hco/3/GRCh38#113589401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44096651-A-C

http://identifiers.org/hco/3/GRCh38#113592929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44094239-C-A

113592980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44094198-A-G

113593089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44094057-T-C

113593759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093701-A-G

http://identifiers.org/hco/3/GRCh38#113594068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44093379-C-A

113594068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093379-C-T

113594120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093336-A-G

113594128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093328-T-A

113594128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093328-T-C

113594245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44093217-A-G

113594877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44093102-T-C

http://identifiers.org/hco/3/GRCh38#113594996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44092989-C-A

113595647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44092486-C-T

113595847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44092285-A-G

113595992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44092144-A-T

113596073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44092063-G-A

113600350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091816-T-C

113600386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091780-C-T

113600619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091548-T-C

113600619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091548-T-G

113600770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091301-G-A

113600820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091262-G-A

113600820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091262-G-T

113600922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44091177-G-A

113601234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44090916-A-G

113601257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44090893-G-A

113601257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44090893-G-T

113601426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090449-T-C

http://identifiers.org/hco/3/GRCh38#113601435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44090440-C-A

113601435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090440-C-T

http://identifiers.org/hco/3/GRCh38#113601436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44090438-A-C

113601436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090438-A-G

113601439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090435-T-G

113601446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090427-T-C

113601506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090371-G-A

113601506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090371-G-C

113601506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090371-G-T

113601555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090323-A-G

113601555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090323-A-T

113601664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090204-G-A

113601703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090163-G-A

113601703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090163-G-T

113601770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090136-A-G

113601815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090089-A-G

113601828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090076-G-A

113601828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090076-G-T

http://identifiers.org/hco/3/GRCh38#113601875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44090039-C-A

113601875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090039-C-G

113601875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090039-C-T

113601895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44090018-T-C

113601947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089522-G-A

113601947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089522-G-T

113601958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089500-G-T

113601971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089487-G-A

113602058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089397-G-A

113602058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089397-G-T

113602064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089391-G-T

http://identifiers.org/hco/3/GRCh38#113602135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44089321-C-A

113602135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089321-C-T

113602242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089214-T-C

113602274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089182-A-G

http://identifiers.org/hco/3/GRCh38#113602294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44089162-C-A

113602294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089162-C-T

113602301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089155-T-A

113602337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089131-A-G

113602343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44089125-G-T

113602383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44089085-A-G

113602394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089066-A-G

113602398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44089062-A-G

113602665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088812-G-C

113602764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088494-T-C

113602805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088457-A-G

113602805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088457-A-T

113602863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088410-G-A

113602903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088370-A-G

113602903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088370-A-T

113602987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44088288-G-A

113603010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088267-T-C

113603052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088225-G-A

113603060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44088217-G-A

113603060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44088217-G-C

113603073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088204-A-G

113603100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088177-T-C

113603103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088174-G-A

113603103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088174-G-C

113603143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088134-G-A

113603143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088134-G-C

113603143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44088134-G-T

113603172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088105-A-G

113603207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088070-A-G

http://identifiers.org/hco/3/GRCh38#113603213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44088064-C-A

113603213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088064-C-T

113603223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088054-T-A

113603223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088054-T-C

http://identifiers.org/hco/3/GRCh38#113603248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44088031-C-A

113603248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088031-C-G

113603263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44088016-T-C

113603366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087925-A-G

113603530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087772-C-G

113603563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087739-A-G

113603563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087739-A-T

113603587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087715-T-C

113603683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087621-A-G

113603894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087493-G-A

113603894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087493-G-C

113603894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087493-G-T

113603916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087471-G-A

113603916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087471-G-C

113603916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44087471-G-T

http://identifiers.org/hco/3/GRCh38#113604102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44087154-C-A

113604116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44087139-G-A

113604116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44087139-G-T

113604119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44087136-T-G

http://identifiers.org/hco/3/GRCh38#113604141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44087114-C-A

113604199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44087065-A-G

113604338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44086930-A-G

http://identifiers.org/hco/3/GRCh38#113604443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44086813-C-A

113604443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44086813-C-G

http://identifiers.org/hco/3/GRCh38#113604777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44086317-C-A

113604777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44086317-C-T

http://identifiers.org/hco/3/GRCh38#113604783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44086311-C-A

113604783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44086311-C-T

113604815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44086279-G-A

113604815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44086279-G-T

113604823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44086271-G-T

113605004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44086085-G-T

113605056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44086036-A-G

113605617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44085259-G-C

http://identifiers.org/hco/3/GRCh38#113605841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44085056-C-A

113605841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44085056-C-T

113605930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084904-T-C

113606046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084728-T-A

113606138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084643-T-C

113606223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084525-G-A

113606343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084404-G-A

113606343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084404-G-T

113606388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44084359-T-C

113606467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44084290-A-G

113606497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44084260-G-A

113606497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44084260-G-T

113606662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44084102-G-T

113606782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083971-T-C

http://identifiers.org/hco/3/GRCh38#113606838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083921-A-C

http://identifiers.org/hco/3/GRCh38#113606840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083919-C-A

113606840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083919-C-T

113606891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083869-G-A

113606951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083810-T-A

113606972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083789-T-G

113606974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083787-G-A

113606974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083787-G-C

113606974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083787-G-T

http://identifiers.org/hco/3/GRCh38#113607009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083752-C-A

113607030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083734-T-C

113607086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083678-C-G

113607086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083678-C-T

113607104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44083660-G-A

113607165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44083601-T-C

http://identifiers.org/hco/3/GRCh38#113607181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083588-C-A

113607181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44083588-C-G

113607181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44083588-C-T

113607194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083533-T-A

113607194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083533-T-C

http://identifiers.org/hco/3/GRCh38#113607206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083521-C-A

113607206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083521-C-G

http://identifiers.org/hco/3/GRCh38#113607250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083478-A-C

113607287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083394-T-A

113607287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083394-T-G

113607297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083371-A-G

113607311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083356-A-G

113607374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083198-T-A

http://identifiers.org/hco/3/GRCh38#113607422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44083152-C-A

113607478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44083082-C-T

113607708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082863-G-T

http://identifiers.org/hco/3/GRCh38#113607949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44082646-C-A

113607949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082646-C-T

113607957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082634-T-G

113608092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 44082505-A-G

113608149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44082448-C-T

http://identifiers.org/hco/3/GRCh38#113608167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44082430-C-A

113608167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44082430-C-G

113608167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44082430-C-T

113608297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082295-T-C

113608351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082244-T-C

113608365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082237-T-A

113608374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082230-A-G

113608404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082196-T-C

113608406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44082194-T-C

113608419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 44082169-G-A

http://identifiers.org/hco/3/GRCh38#113608599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44081989-C-A

113608599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081989-C-T

http://identifiers.org/hco/3/GRCh38#113608673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44081914-A-C

113608947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081456-G-A

113608986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081425-A-G

113609028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081383-C-T

113609548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081192-G-A

113609548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44081192-G-T

http://identifiers.org/hco/3/GRCh38#113610342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44080755-C-A

113610408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44080689-A-T

113610802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44080111-G-A

113610860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44080050-T-C

http://identifiers.org/hco/3/GRCh38#113611052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44079886-C-A

113611052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44079886-C-G

113611052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44079886-C-T

113611100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44079838-T-C

113611133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44079805-G-A

113611133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44079805-G-C

113612022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078464-G-A

113612022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078464-G-T

113612036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078450-G-A

113612080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44078408-T-C

113612080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44078408-T-G

113612200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078288-T-C

113612247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078260-A-G

113612247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078260-A-T

113612267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078238-A-T

113612283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078222-T-A

113612283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078222-T-C

113612319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078192-G-T

113612380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078142-G-T

http://identifiers.org/hco/3/GRCh38#113612389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44078139-C-A

113612389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078139-C-T

113612410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44078118-G-T

http://identifiers.org/hco/3/GRCh38#113612428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44078101-A-C

113612536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077852-G-A

113612718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077693-C-G

113612718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077693-C-T

http://identifiers.org/hco/3/GRCh38#113612769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44077642-C-A

113613020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077339-G-C

113613021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077338-G-C

113613302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44077113-A-G

113614610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076746-T-C

http://identifiers.org/hco/3/GRCh38#113614618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44076738-C-A

113614915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076486-A-G

113614915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076486-A-T

113614977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076426-A-G

113614985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076418-A-T

113615088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076317-G-T

113615101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076304-G-C

113615167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076250-A-T

http://identifiers.org/hco/3/GRCh38#113615170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44076247-C-A

113615206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076212-G-A

113615206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076212-G-T

http://identifiers.org/hco/3/GRCh38#113615207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44076211-C-A

113615207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44076211-C-T

113615534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075908-T-G

113615801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075662-G-A

113615881-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075608-T-A

113615881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075608-T-C

http://identifiers.org/hco/3/GRCh38#113615899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44075590-A-C

113615899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075590-A-G

113615899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075590-A-T

http://identifiers.org/hco/3/GRCh38#113615917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44075571-C-A

113615941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075547-A-G

113615941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075547-A-T

113616018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075464-G-T

113616215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075273-A-T

113616228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075260-A-G

113616244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075244-T-G

113616361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44075133-A-T

113617252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44074068-A-G

http://identifiers.org/hco/3/GRCh38#113617304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44074010-A-C

113617304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44074010-A-T

113617343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44073962-G-A

113617362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44073948-G-A

113617451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44073846-C-G

113617623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44073686-C-T

113617643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44073666-C-T

113617898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44073492-A-G

113617898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44073492-A-T

113618016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44073433-A-T

113618085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44073372-C-T

http://identifiers.org/hco/3/GRCh38#113618326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44073143-C-A

113618326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44073143-C-T

113618464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44072431-A-G

http://identifiers.org/hco/3/GRCh38#113618473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44072422-A-C

113618473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44072422-A-G

113618496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44072383-G-A

113619330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071852-C-T

113619533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071683-A-T

113619739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44071507-A-G

http://identifiers.org/hco/3/GRCh38#113619764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44071482-A-C

113619764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44071482-A-G

113619765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44071481-A-G

113619913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44071099-A-G

113619913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44071099-A-T

113619924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071057-G-A

113619924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071057-G-T

113619985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071011-T-C

113619994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071003-G-A

113619994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44071003-G-T

113620073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070926-T-A

113620211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070799-T-C

113620211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070799-T-G

113620215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070795-T-A

113620373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070628-T-C

113620485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44070523-G-A

113622618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44066574-G-A

113622618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44066574-G-T

113623408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44065818-A-G

http://identifiers.org/hco/3/GRCh38#113623414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44065812-C-A

113623414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44065812-C-T

113623647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44065582-C-T

http://identifiers.org/hco/3/GRCh38#113623766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44065468-C-A

113623766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44065468-C-G

113623766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44065468-C-T

http://identifiers.org/hco/3/GRCh38#113623774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44065460-C-A

113623774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44065460-C-T

http://identifiers.org/hco/3/GRCh38#113625998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44064040-C-A

113625998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44064040-C-T

113626011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44064032-T-C

113626013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44064030-G-A

113626013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44064030-G-T

113626036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44064007-A-G

http://identifiers.org/hco/3/GRCh38#113626053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44063991-C-A

113626073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44063971-T-C

113626073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44063971-T-G

http://identifiers.org/hco/3/GRCh38#113626096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44063949-C-A

113626096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44063949-C-G

113626105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44063939-A-G

113626105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44063939-A-T

113626108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44063936-C-G

http://identifiers.org/hco/3/GRCh38#113626131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44063913-C-A

113626131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44063913-C-T

113626239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063818-T-C

http://identifiers.org/hco/3/GRCh38#113626321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44063749-C-A

113626322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063748-T-G

http://identifiers.org/hco/3/GRCh38#113626326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44063744-C-A

113626365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063697-T-A

113626546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063499-A-G

113626547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063498-T-C

113626602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063446-C-G

113627035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44063107-T-C

113627042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44063100-G-A

113627084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44063059-G-A

113627863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061844-G-A

113627863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061844-G-T

113627878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061830-G-A

113627878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061830-G-C

113627894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061817-G-T

113627895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061816-G-A

113627895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061816-G-T

113628151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061624-T-C

113628177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061563-A-G

113628181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061559-T-C

113628227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061512-T-C

113628230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061509-T-C

113628230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061509-T-G

http://identifiers.org/hco/3/GRCh38#113628277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44061459-C-A

113628278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061458-T-G

http://identifiers.org/hco/3/GRCh38#113628311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44061438-A-C

113628316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061433-G-T

113628328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061421-G-A

113628328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061421-G-T

113628361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061395-G-T

http://identifiers.org/hco/3/GRCh38#113628431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44061326-C-A

113628445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061312-T-C

113628525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061235-A-T

113628565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061204-A-G

http://identifiers.org/hco/3/GRCh38#113628597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44061180-C-A

113628615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061162-G-A

113628615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061162-G-T

http://identifiers.org/hco/3/GRCh38#113628740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44061061-C-A

113628740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061061-C-T

113628781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44061027-T-C

113628837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060973-T-C

113628860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060939-C-T

113628862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060937-G-T

http://identifiers.org/hco/3/GRCh38#113628882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44060924-C-A

113628882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060924-C-T

http://identifiers.org/hco/3/GRCh38#113628932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44060856-C-A

113628998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060791-T-C

113629120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060669-G-T

113629146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060636-T-C

http://identifiers.org/hco/3/GRCh38#113629292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44060487-C-A

113629292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060487-C-T

113629432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060340-G-A

113629443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060329-A-G

113629529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060283-C-T

113629573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44060245-T-C

http://identifiers.org/hco/3/GRCh38#113629711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44060107-A-C

113629711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44060107-A-T

113629805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059994-G-C

113629843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059962-C-T

113629869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059935-C-T

113629918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059885-A-G

113630031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059781-G-C

113630285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059533-A-G

113630586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059229-G-A

113630616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44059195-G-A

113631024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44058743-C-T

113631247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44058551-A-G

113631249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44058548-A-G

113631589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44058225-T-C

113632226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44057284-A-G

113632285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44057232-G-C

113632323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25967
most severe consequence: intron variant
orthologous variants: 44057195-C-T