53979265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294636-A-G

53979326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294572-T-C

53979342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294566-G-C

http://identifiers.org/hco/6/GRCh38#53979513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77294413-C-A

53979656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294229-A-T

53979760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77294145-G-A

http://identifiers.org/hco/6/GRCh38#53981995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77293870-C-A

53981995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77293870-C-T

53982467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291810-T-C

53982470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291807-A-G

53982523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291748-G-A

53982634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291636-G-C

http://identifiers.org/hco/6/GRCh38#53982646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77291624-C-A

53982680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291590-T-A

53982680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291590-T-C

53982771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77291482-T-C

53982842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 77291411-G-A

53982860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291389-A-T

53982909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291336-G-T

53983016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77291109-T-G

53983126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290952-A-G

53983129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290949-T-C

53983193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290892-G-A

53983194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290891-T-C

53983755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290744-G-A

53983755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290744-G-T

53983890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77290577-A-T

http://identifiers.org/hco/6/GRCh38#53984634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77289218-A-C

53984687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77289166-A-G

53984982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77288888-G-A

http://identifiers.org/hco/6/GRCh38#53985602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77287793-C-A

53985602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287793-C-T

53985810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287603-A-T

53985836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77287577-T-C

53986385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77287052-A-G

53986530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285679-C-T

53986627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285599-T-C

53986675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285536-G-T

53986821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285443-G-A

53986821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285443-G-T

53987095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77285081-A-T

53987311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284877-C-T

53987473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284729-A-G

53987739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284522-G-A

53987740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284521-C-T

http://identifiers.org/hco/6/GRCh38#53987787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77284510-A-C

53987931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284449-A-G

53988230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284187-T-A

53988230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284187-T-G

53988284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77284137-T-C

53988815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283574-T-A

53988815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283574-T-G

53988830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283559-T-G

53988949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283454-C-T

http://identifiers.org/hco/6/GRCh38#53988951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77283452-C-A

53988951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283452-C-T

53988970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283433-G-A

53988970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283433-G-T

53989055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77283364-T-G

53989163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283247-T-A

53989214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283197-C-T

53989282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283133-A-G

53989375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77283036-C-G

53989762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282741-C-G

53989762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282741-C-T

53989787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282716-A-G

53989866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282298-G-T

http://identifiers.org/hco/6/GRCh38#53989887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77282284-C-A

http://identifiers.org/hco/6/GRCh38#53989919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77282261-C-A

53989919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282261-C-T

53989991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282200-T-C

53990044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282150-G-A

53990198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77282006-C-T

53990268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281955-C-T

53990304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281919-G-A

53990304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281919-G-T

53990524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281706-G-C

53990556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281632-T-G

53990686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281499-T-A

53990777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281426-T-A

53990799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77281392-T-C

53993917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77278080-T-C

53994085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277941-A-G

53994171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277871-G-C

53994408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277650-C-T

53994545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277514-G-A

53994622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277426-T-G

53994638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277409-G-A

53994643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277404-G-A

53994643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277404-G-T

53994681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277373-G-T

53994698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77277360-C-T

53995342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276961-C-T

53995415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276893-A-G

http://identifiers.org/hco/6/GRCh38#53995783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276563-C-A

53995783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276563-C-T

53995806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276541-T-A

53995862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276498-A-G

53995976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276412-T-C

http://identifiers.org/hco/6/GRCh38#53996047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276352-C-A

53996120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276289-T-C

http://identifiers.org/hco/6/GRCh38#53996142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276263-A-C

53996143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276262-T-C

53996188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276218-G-C

53996226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276183-G-A

53996288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276127-T-C

http://identifiers.org/hco/6/GRCh38#53996347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276077-C-A

http://identifiers.org/hco/6/GRCh38#53996374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77276053-C-A

53996374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77276053-C-T

53996578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275843-G-T

53996717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275694-G-A

53996729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275681-A-T

53996758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275656-A-G

53996795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275617-T-C

53996822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275590-G-A

53996863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275542-A-T

53996884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275521-A-G

53996884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275521-A-T

53996972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275458-T-C

53997057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275378-G-A

53997057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275378-G-T

53997092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275340-C-T

53997312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275101-T-C

53997322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275091-T-C

53997389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77275028-G-A

53997674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274245-A-T

53997957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77274001-A-G

53997964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273994-G-A

53997964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273994-G-T

53998073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273904-T-C

53998145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273825-C-T

53998250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273752-T-C

53998259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273747-A-G

53998286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273720-G-A

53998370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273636-C-T

53998495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273479-A-G

53998674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273232-G-C

53998752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273160-T-C

53998827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273084-G-A

53998827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77273084-G-T

http://identifiers.org/hco/6/GRCh38#53999115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77272757-C-A

53999115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77272757-C-T

54000559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271445-T-A

54000559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271445-T-G

54000595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271415-G-A

http://identifiers.org/hco/6/GRCh38#54000779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77271238-C-A

54000813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271223-G-C

54000846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-A

54000846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-C

54000846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271190-T-G

54000870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271160-T-C

54000883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77271149-G-T

54001041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77270994-C-T

http://identifiers.org/hco/6/GRCh38#54001115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77270923-C-A

54001461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270681-G-T

54001534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270615-G-A

54001742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270410-G-A

54001879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270294-A-G

54002087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77270102-A-T

54002986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268226-T-C

54003045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268172-T-A

54003068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268159-G-C

54003068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268159-G-T

54003071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268153-T-C

http://identifiers.org/hco/6/GRCh38#54003106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77268117-A-C

54003141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268083-T-A

54003153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77268071-G-A

http://identifiers.org/hco/6/GRCh38#54003155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77268069-A-C

54003474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77267888-G-T

http://identifiers.org/hco/6/GRCh38#54004327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77267352-C-A

54004809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266890-A-G

54004818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266881-A-G

54004844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266841-C-T

54004872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266813-G-A

54005328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77266688-G-A

54007586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262648-G-A

54007586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262648-G-T

54007758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262476-A-G

54008603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262235-G-A

54008604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262234-G-T

54008764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262108-T-C

http://identifiers.org/hco/6/GRCh38#54008800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77262072-C-A

54008800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262072-C-G

54008859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77262019-T-A

54009154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261652-G-A

54009157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261649-C-G

54009157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261649-C-T

54009265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261546-T-G

54009345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77261484-G-T

54009986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260841-T-A

54010002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260822-C-T

54010506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260444-G-A

54010578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260371-T-G

54010612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260340-A-G

54010732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260244-A-T

54010772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260213-C-T

54010863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260123-C-G

54010866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77260120-A-G

54011084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259910-A-G

54011153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259845-G-A

54011178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259801-C-T

54011407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259587-T-G

54011414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259580-G-A

54011437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259491-G-C

54011551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259386-A-G

54011602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259344-T-A

54011807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77259154-T-C

54012064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258277-A-T

54012084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258257-A-T

54012144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258206-T-A

54012258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77258105-A-G

http://identifiers.org/hco/6/GRCh38#54012366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77258002-A-C

54012497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257843-C-G

http://identifiers.org/hco/6/GRCh38#54012899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77257127-C-A

54012945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77257081-T-C

54013214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256780-G-A

54013664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256391-G-C

54013758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256302-T-A

54017881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256160-G-T

54017915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77256129-A-G

54018006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256055-G-A

54018006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256055-G-T

54018063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77256017-G-A

http://identifiers.org/hco/6/GRCh38#54018075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77256005-C-A

54018112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77255984-A-G

54018225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255863-G-T

54018904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77255174-T-A

54018990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77255088-T-C

54019037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77255035-T-C

54019081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77254985-A-G

54019171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254893-T-C

54019225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254841-A-T

54019236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254831-G-A

54019236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254831-G-T

54019334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254734-T-G

54019561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254498-C-G

54019674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254387-C-T

54019965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77254108-T-C

54020094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253991-G-A

54020319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253771-T-G

54020353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253643-C-T

54020358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253639-G-A

54020760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253270-T-C

54020826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253203-G-A

54020907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253120-G-A

54020950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253094-C-T

54021018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77253025-A-G

54021343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252724-G-A

54021451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252632-A-G

54021696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77252032-G-T

54021891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251855-G-A

54021999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251747-T-G

54022073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251679-T-G

54022096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251657-A-G

54022133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251619-A-G

54022319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251456-A-T

54022452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251327-G-C

54022783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77251008-G-C

54022842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250947-C-T

54023247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250874-A-G

54023258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250863-A-G

54023446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250714-A-G

http://identifiers.org/hco/6/GRCh38#54023448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77250712-A-C

54024357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250476-A-G

54024505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250354-G-A

54024644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77250242-T-C

54025312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249929-T-C

54025433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249843-G-T

http://identifiers.org/hco/6/GRCh38#54025566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77249754-A-C

54025566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249754-A-G

54025602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249717-T-A

54025638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249679-G-A

54025639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249678-T-A

54025639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249678-T-C

54025663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249648-C-T

54025689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249626-A-G

54025733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249593-T-A

54025780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249549-A-G

54026058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249275-G-A

http://identifiers.org/hco/6/GRCh38#54026071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77249262-C-A

54026088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77249245-G-A

54026414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248927-T-C

54026415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248926-T-G

54026450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248892-G-T

54026609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248774-T-C

54026652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248734-G-A

54026652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248734-G-T

54026797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248645-C-T

54026845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248598-A-T

54026955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248492-C-T

54027049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248422-G-A

54027284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248188-G-A

54027284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248188-G-T

54027320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248155-C-T

54027512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248015-G-A

54027512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77248015-G-T

54027581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247946-G-A

54027581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247946-G-T

54027942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247569-T-C

54027944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247564-C-T

54028026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247487-T-G

54028523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77247018-G-A

54028579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246971-C-T

54028629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246923-T-C

54028652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246858-T-C

54028660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246850-C-T

54028734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246713-G-A

54028747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246700-A-G

54028747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246700-A-T

54028779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246679-T-C

54028864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246602-A-G

54028871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77246592-T-A

54028888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246580-T-C

54028943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77246534-G-A

54029216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245886-G-T

54029305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245795-T-C

54029309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245791-A-G

54029309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245791-A-T

54029316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245784-A-G

54029351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245750-G-A

54029351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245750-G-T

54029360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245741-G-A

54029360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245741-G-C

54029361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245740-A-G

54029361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245740-A-T

54029396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245726-A-G

54029396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245726-A-T

http://identifiers.org/hco/6/GRCh38#54029435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77245687-C-A

http://identifiers.org/hco/6/GRCh38#54029439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77245683-C-A

54029441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77245681-T-C

54029475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245647-A-G

54029535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245564-T-C

54029588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245518-A-G

54029591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77245515-G-C

54030375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244904-T-C

54030448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244852-G-A

54030487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244815-T-C

54030565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244713-C-T

http://identifiers.org/hco/6/GRCh38#54030677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77244577-C-A

54030721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244543-T-C

54030743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77244530-G-T

54031392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77243472-A-G

54031404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243459-C-T

54031449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243413-G-A

54031449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243413-G-T

54031493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243370-T-C

54031514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243348-G-T

54031537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243325-C-T

54031540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77243322-G-T

54031658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77243131-C-G

54031658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77243131-C-T

54031971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242804-C-T

54031984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77242768-C-T

54037640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 77234503-T-C

54037778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234358-C-T

http://identifiers.org/hco/6/GRCh38#54037830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77234319-A-C

54037907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234257-A-G

54037944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234219-A-T

54038141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234033-G-A

54038143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77234031-A-G

54038288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233888-G-A

54038502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233742-T-G

54038533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233713-T-C

54038616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233640-T-C

54038653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233600-A-G

54038706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77233547-C-T

http://identifiers.org/hco/6/GRCh38#54039036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77233238-C-A

54039367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232915-G-A

54039367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232915-G-T

54039382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232899-G-A

54039382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232899-G-C

54039701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77232566-G-A

54042240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77231211-G-A

54042419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77231026-G-T

54042482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230963-C-T

54042606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230817-T-C

54042633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230789-G-A

54042660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230762-G-A

54042700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230727-T-C

54042719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77230708-G-A

54043535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229527-A-G

54043540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77229522-G-T

54043947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227840-G-C

54044210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227458-T-G

54044220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227448-T-C

54044361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227320-C-T

54044646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227006-T-C

54044646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77227006-T-G

54044665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226988-A-G

54044665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226988-A-T

54045011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77226042-T-G

54045468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225895-G-A

54045468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225895-G-C

54045521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225841-G-A

54046076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225741-T-A

http://identifiers.org/hco/6/GRCh38#54046126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225693-C-A

http://identifiers.org/hco/6/GRCh38#54046127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225692-C-A

54046127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225692-C-G

54046127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225692-C-T

http://identifiers.org/hco/6/GRCh38#54046208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225616-A-C

54046239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225594-A-G

http://identifiers.org/hco/6/GRCh38#54046265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77225575-C-A

54046265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225575-C-T

54046345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77225490-A-G

http://identifiers.org/hco/6/GRCh38#54046693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224895-C-A

54046733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224852-T-C

54046734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224851-G-A

http://identifiers.org/hco/6/GRCh38#54046744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224841-C-A

54046982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77224620-G-T

54047212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77224438-A-G

54047244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77224407-A-G

54047292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 77224356-C-T

http://identifiers.org/hco/6/GRCh38#54047312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77224318-C-A

54047541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77223523-T-A

54047541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 77223523-T-C

54048186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223201-T-G

54048232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223146-T-C

54048610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77223028-T-C

54048917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222681-T-G

54049250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222425-T-C

54049307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222368-A-T

54049441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222236-G-T

54049564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222127-C-G

54049607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77222085-C-G

54049682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77221993-C-T

54050657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220597-A-T

54050738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220520-G-T

54050968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220306-G-A

54050977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220297-C-T

http://identifiers.org/hco/6/GRCh38#54050995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220280-C-A

http://identifiers.org/hco/6/GRCh38#54050999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220276-C-A

54051214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77220100-T-C

http://identifiers.org/hco/6/GRCh38#54051283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77220042-C-A

54051582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219738-A-T

54051595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219687-T-G

http://identifiers.org/hco/6/GRCh38#54051693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77219595-C-A

54051693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219595-C-T

54051779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219525-A-T

54051962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219302-T-C

54052053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219210-T-C

54053143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219162-T-C

54053198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219109-G-A

54053291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77219021-A-T

54053433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218876-T-C

http://identifiers.org/hco/6/GRCh38#54053648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77218629-A-C

54053680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218593-T-C

54053764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218512-A-G

54054187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218090-C-T

54054220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77218058-C-T

54054421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217858-A-G

54054431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217848-A-T

54054457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217825-C-G

54054478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217803-A-G

54054486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217795-T-C

54055221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217010-T-C

http://identifiers.org/hco/6/GRCh38#54055224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77217007-A-C

54055224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77217007-A-G

54055641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216508-G-C

54055749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216387-A-G

54055796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77216339-G-A

http://identifiers.org/hco/6/GRCh38#54056329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77215801-A-C

54056329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215801-A-T

54056559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215581-T-C

54056587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215553-G-A

54056610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215530-A-G

54056677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215463-C-G

54056835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215320-A-G

54057036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215136-T-C

54057071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77215101-T-C

54057255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214921-A-G

54057270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77214905-G-A

54057437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77213906-G-A

54057553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77213791-A-G

54058822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212942-C-T

54058826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77212938-A-G

http://identifiers.org/hco/6/GRCh38#54058933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77212865-A-C

54058933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77212865-A-T

54058953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77212851-A-G

54058971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 77212833-C-T

http://identifiers.org/hco/6/GRCh38#54059001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77212809-A-C

54059314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211532-T-C

54059374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77211498-A-G

54060021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210959-A-G

54060023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210957-G-A

54060023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210957-G-T

54060224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210762-G-T

54060617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210395-T-A

54060643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77210363-G-A

54061030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209991-C-T

54061275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209774-G-A

54061288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77209761-A-G

http://identifiers.org/hco/6/GRCh38#54061641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77209034-C-A

54061823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208872-C-T

54061824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208871-T-C

54061846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208855-G-A

54062109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208586-T-C

54062175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208523-A-G

54062186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208512-A-G

54063757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208232-G-A

54063757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208232-G-T

54063905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77208101-A-G

54064751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77206096-T-G

54067144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77204912-G-A

54067171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77204853-T-C

54068778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77203832-A-T

http://identifiers.org/hco/6/GRCh38#54068955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77203638-A-C

54068955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77203638-A-G

54069980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77202579-C-G

54070067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201326-C-T

54070117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201285-T-C

54070160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201248-T-C

54070230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201174-C-T

54070358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201046-T-A

54070358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77201046-T-C

54070426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200979-G-T

54070499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200916-T-C

54072672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77200050-C-T

54073201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77199521-T-C

http://identifiers.org/hco/6/GRCh38#54073351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#77199415-A-C

54074070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198844-C-T

54074163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198762-T-G

54074220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198704-G-A

54074363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198562-G-A

54074373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198552-T-A

54074506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198411-A-G

54074588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198327-G-A

54074588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198327-G-T

54074822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77198086-A-G

54075011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197946-G-T

54075675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197601-G-A

54075755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197544-G-T

54075804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197510-C-T

54075818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197496-T-C

54075914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77197401-T-G

54076374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196958-A-G

54076471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196888-A-G

54076590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196775-T-C

54076669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196705-T-C

54076752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196179-A-G

54076762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196169-T-G

54076891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77196043-A-G

54077034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195851-A-G

54077261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195635-A-G

54077276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195620-A-G

54077348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195554-A-G

54077372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77195530-T-C

54078233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40963
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77194835-C-T