http://identifiers.org/hco/4/GRCh38#55949003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76736732-C-A

55949003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76736732-C-T

http://identifiers.org/hco/4/GRCh38#55949010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76736739-C-A

55949010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76736739-C-G

55949030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76736759-A-G

55949095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736806-G-A

55949095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736806-G-C

55949095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736806-G-T

55949097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736808-C-T

55949125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736831-G-A

55949140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736845-G-A

55949140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76736845-G-T

55949209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736892-G-A

55949209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76736892-G-T

http://identifiers.org/hco/4/GRCh38#55949249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76736916-A-C

55949517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737057-A-G

55949666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737138-A-G

55949833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737256-G-C

55950011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737396-T-G

55950067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737444-C-G

55950330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76737671-T-C

55950442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76737769-A-G

55950812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738220-G-A

55950934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738350-G-A

55951626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738951-A-G

55951665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738990-A-G

55951668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76738993-G-A

55952017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76739531-T-G

55952093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76739569-A-G

55952097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76739573-T-C

http://identifiers.org/hco/4/GRCh38#55952124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76739600-A-C

55952124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76739600-A-G

55952256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739731-A-G

55952272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739747-T-G

55952317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739793-T-A

55952317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739793-T-C

55952376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739843-T-C

http://identifiers.org/hco/4/GRCh38#55952405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76739885-A-C

55952405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739885-A-G

55952415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739895-T-C

55952415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739895-T-G

55952433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739904-C-T

55952462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739917-G-T

55952501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76739952-T-C

55953028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76740980-T-C

55953061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741012-T-C

55953091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76741045-A-G

55953301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741264-A-G

55953608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741415-A-G

55953755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741512-A-G

55954098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741790-G-A

55954098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741790-G-T

55954104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741796-G-C

55954104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741796-G-T

http://identifiers.org/hco/4/GRCh38#55954115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76741807-A-C

55954128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741820-G-A

55954129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741821-A-T

http://identifiers.org/hco/4/GRCh38#55954198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76741852-A-C

55954198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76741852-A-G

http://identifiers.org/hco/4/GRCh38#55954225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76741879-C-A

55954225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76741879-C-T

55956242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742352-G-A

55956354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76742443-C-G

55957452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76743582-A-G

http://identifiers.org/hco/4/GRCh38#55957465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76743595-C-A

55957465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76743595-C-T

55957521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76743656-T-C

55957776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76743897-G-A

55957783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76743904-T-A

55958473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76744268-A-G

55958603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76744393-G-T

55959657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76745137-G-T

55959674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76745154-C-G

http://identifiers.org/hco/4/GRCh38#55959783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76745304-C-A

http://identifiers.org/hco/4/GRCh38#55959856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76745377-C-A

55959856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76745377-C-T

55959896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76745418-T-C

55960523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76747289-G-A

http://identifiers.org/hco/4/GRCh38#55960528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76747294-C-A

55960528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76747294-C-T

55961091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747746-G-A

55961091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747746-G-T

55961094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747749-T-C

55961095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747750-C-T

55961329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76747968-C-T

55961394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76748017-T-C

55964123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749089-T-C

http://identifiers.org/hco/4/GRCh38#55964143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76749104-C-A

55964143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749104-C-T

55964174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749137-T-C

55964256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749214-G-A

http://identifiers.org/hco/4/GRCh38#55964342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76749302-C-A

55964342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76749302-C-T

55964378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 76749338-G-A

55964449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749411-A-G

55964449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749411-A-T

55964487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749435-G-A

55964512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749500-G-T

55964544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76749681-G-T

55964753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76750041-G-T

http://identifiers.org/hco/4/GRCh38#55964754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76750042-C-A

55964754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76750042-C-T

55965250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750581-G-T

http://identifiers.org/hco/4/GRCh38#55965262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76750591-C-A

55965262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750591-C-G

55965262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750591-C-T

55965360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750688-A-G

55965361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750689-T-A

55965397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750727-G-T

55965496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750824-T-C

55965548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76750881-T-C

55966002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751621-G-A

55966002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751621-G-T

55966040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751659-A-G

55966047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751666-T-G

55966050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751669-G-T

55966061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751679-G-A

55966061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751679-G-T

http://identifiers.org/hco/4/GRCh38#55966078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76751695-C-A

55966078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751695-C-G

55966135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751751-T-G

55966348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751868-T-A

55966348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751868-T-C

55966348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751868-T-G

55966377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76751881-A-G

http://identifiers.org/hco/4/GRCh38#55966415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76751900-C-A

http://identifiers.org/hco/4/GRCh38#55966575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76751986-C-A

55966849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752201-T-G

http://identifiers.org/hco/4/GRCh38#55966990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76752331-A-C

55967122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752430-A-G

55967614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752856-C-T

55967625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76752867-T-C

55967983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753411-T-C

55968038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753464-G-T

55968141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753604-A-G

55968408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753827-T-A

55968408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753827-T-C

55968426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76753845-A-G

55968508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754010-G-T

55968513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754014-A-G

55968797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754318-A-G

55968816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754339-G-T

55968926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754436-A-G

55968950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754462-T-G

55968999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754505-T-C

55969192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754690-G-A

55969223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754720-G-C

55969223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754720-G-T

55969244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754743-T-A

55969244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754743-T-C

55969244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754743-T-G

55969245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754744-G-A

55969245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754744-G-T

http://identifiers.org/hco/4/GRCh38#55969258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76754751-C-A

55969258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754751-C-G

55969258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754751-C-T

55969388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754847-T-C

55969486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754863-T-C

55969510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754887-C-G

55969608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754982-A-G

55969608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76754982-A-T

55971275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76757483-G-T

55971462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76757624-A-G

55974394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759157-A-G

55974584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759350-T-C

55974704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759459-G-A

55974735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76759486-T-G

55974789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76759540-T-C

55974877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76759628-C-G

http://identifiers.org/hco/4/GRCh38#55974904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76759655-C-A

55974904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76759655-C-G

55974904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76759655-C-T

55976532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76760597-T-C

http://identifiers.org/hco/4/GRCh38#55977293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76761062-A-C

55977376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761176-T-G

55977378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761178-T-A

55978163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761806-G-A

55978252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76761855-C-T

55979122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762683-A-G

55979304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762797-C-G

55979306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762799-C-T

55979458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762896-T-G

55979463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762901-A-G

55979555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76762992-A-G

55979669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763056-A-G

http://identifiers.org/hco/4/GRCh38#55979684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76763071-A-C

55979727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763102-C-T

55979993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763335-A-G

55980006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763348-A-T

55980056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763392-G-A

55980056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763392-G-T

55980094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763421-T-C

55980318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763660-G-A

55980318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763660-G-T

55980388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763701-T-C

55980490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76763775-T-C

55981079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76764513-T-A

55981244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76764667-T-C

55981244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76764667-T-G

55981322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76764745-G-A

55981331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76764754-C-T

55981355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76764778-G-A

55982861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766185-A-G

55982956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766276-G-A

55983020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766336-A-T

55983310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766622-G-A

55983310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76766622-G-T

55984821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76768605-G-A

55984965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76768870-G-A

55985021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76768922-A-G

55985021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76768922-A-T

55985161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769029-T-G

55985202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769062-T-A

55985202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769062-T-C

55985313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76769163-A-G

55985378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769225-T-C

55985381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769228-G-A

55985381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769228-G-T

55985398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769235-T-C

55985431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76769271-T-A

55991463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76771893-A-G

55991960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76772500-G-T

55992134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772679-G-A

55992185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772725-A-G

55992185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772725-A-T

http://identifiers.org/hco/4/GRCh38#55992211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76772751-A-C

55992211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76772751-A-G

55992698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76773191-C-G

55992756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76773243-A-G

55992933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76773436-G-A

http://identifiers.org/hco/4/GRCh38#55993069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76773738-A-C

55993473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774051-C-T

55993548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774136-G-A

55993619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774205-A-G

55993797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774375-A-G

55993851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774414-T-A

55993851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774414-T-C

55993851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774414-T-G

55994086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774709-A-G

55994185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774803-A-G

55994187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774805-T-A

55994187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774805-T-C

55994604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76774899-A-G

55995848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775562-A-G

55995938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76775736-C-T

http://identifiers.org/hco/4/GRCh38#55996067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76775876-A-C

55996391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776190-C-T

http://identifiers.org/hco/4/GRCh38#55996737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76776478-C-A

55996737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776478-C-T

http://identifiers.org/hco/4/GRCh38#55996738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76776479-C-A

55996738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776479-C-T

55996858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776593-C-T

55996916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776652-A-G

55996947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776683-A-G

55996970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76776714-A-T

55997690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777306-G-A

55997866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777441-A-G

55998114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777659-C-T

55998235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777769-A-T

55998384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777910-A-G

55998384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777910-A-T

55998401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777932-C-T

55998442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777971-C-T

55998462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76777991-G-C

55998477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778006-T-C

55998927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778147-A-G

55999192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778409-A-G

55999291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778504-T-C

55999305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76778515-A-G

55999305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76778515-A-T

55999324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76778534-C-T

55999333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76778543-G-C

55999472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76778682-C-G

55999561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76778770-T-C

http://identifiers.org/hco/4/GRCh38#55999627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76778836-A-C

55999627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76778836-A-G

http://identifiers.org/hco/4/GRCh38#55999655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76778864-C-A

55999655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778864-C-T

56008048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76778998-A-G

56008076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779025-G-A

56008493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779427-A-G

56008617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779513-T-C

56008724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779617-T-C

56009610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779909-A-T

56009616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779915-A-G

56009616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779915-A-T

56009656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76779939-T-G

56009908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780179-G-A

56009924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780194-T-C

http://identifiers.org/hco/4/GRCh38#56009967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76780230-C-A

56009967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780230-C-T

56010732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76780786-A-G

56011283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781384-A-G

http://identifiers.org/hco/4/GRCh38#56011357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76781445-A-C

56011358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781446-A-T

56011366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781454-T-C

56011404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76781512-A-T

56011525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781633-G-A

56011525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781633-G-T

56011537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781645-T-G

56011546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781654-A-T

56011559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781677-G-A

56011559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781677-G-T

http://identifiers.org/hco/4/GRCh38#56011654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76781783-C-A

56011654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781783-C-T

56011736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781940-G-T

56011761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76781961-A-G

http://identifiers.org/hco/4/GRCh38#56011797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76781996-C-A

56011797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76781996-C-T

56016503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76783867-T-C

56017031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784116-G-A

56017113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784197-A-T

56017563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784616-A-G

http://identifiers.org/hco/4/GRCh38#56017638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76784699-C-A

56017638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784699-C-T

http://identifiers.org/hco/4/GRCh38#56017686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76784747-A-C

56017686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76784747-A-G

56017753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76784814-G-A

56017753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76784814-G-C

56017893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784939-T-C

56017899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784945-C-G

56017899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784945-C-T

56017909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784954-T-A

56017948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784968-G-T

http://identifiers.org/hco/4/GRCh38#56017968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76784988-C-A

56017968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76784988-C-T

56017988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785010-T-C

56018009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785027-G-A

56018009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785027-G-T

56018384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785172-G-A

56018384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785172-G-T

56018401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785188-A-G

56018725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785389-A-G

56019259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785829-G-T

56019304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785866-A-G

56019310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76785872-T-C

56019373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76785931-T-C

56020176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786407-G-A

56020360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786552-A-T

56020383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786560-G-A

56020653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786737-T-C

56020676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 76786769-A-G

http://identifiers.org/hco/4/GRCh38#56020775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#76786868-C-A

56020775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 76786868-C-G

56020775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76786868-C-T

http://identifiers.org/hco/4/GRCh38#56020837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76786927-C-A

56020854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786944-G-A

56020854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76786944-G-T

http://identifiers.org/hco/4/GRCh38#56024349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76788224-A-C

56024349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788224-A-G

56024463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788701-G-A

56024463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788701-G-T

56024582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76788810-T-C

56024689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76788912-G-A

56026440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789780-G-T

56026504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76789840-T-C

56026755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790061-G-A

56026755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790061-G-C

56026845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790141-G-A

56026931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790233-A-G

56026989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790289-G-A

56027329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790584-A-G

56027436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76790691-A-G

http://identifiers.org/hco/4/GRCh38#56028338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76791249-A-C

56028736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76791603-T-C

56031270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792409-A-G

56031321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76792455-T-C

http://identifiers.org/hco/4/GRCh38#56031451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76792567-C-A

56031745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76792861-A-G

56032537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76793774-C-G

56032589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76793821-C-T

56032665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76793901-A-G

56032805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794062-C-T

http://identifiers.org/hco/4/GRCh38#56032815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76794072-A-C

56032843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794095-G-A

56032843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794095-G-C

56032843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794095-G-T

56032895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794138-T-C

56032896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794139-T-C

56032999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794245-T-C

56033097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 76794343-A-G

56033253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29086
most severe consequence: 3 prime UTR variant
orthologous variants: 76794490-A-G