83641862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91926192-A-T

83641864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91926190-T-A

83645149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91925340-G-A

83645262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91925226-T-C

83645318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91925144-G-C

http://identifiers.org/hco/11/GRCh38#83645382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91925092-A-C

83645437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91925050-A-G

83645758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924719-G-T

83645870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924607-T-C

83645907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924573-G-T

83645935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924547-G-A

83645935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924547-G-T

83645954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924528-G-A

83645954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924528-G-T

83646188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91924289-A-G

http://identifiers.org/hco/11/GRCh38#83646486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923689-C-A

83646498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923677-T-C

83646509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923666-C-T

http://identifiers.org/hco/11/GRCh38#83646538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923644-C-A

http://identifiers.org/hco/11/GRCh38#83646540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923642-C-A

83646540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923642-C-G

http://identifiers.org/hco/11/GRCh38#83646543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923639-C-A

83646543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923639-C-T

83646602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923581-C-T

http://identifiers.org/hco/11/GRCh38#83646758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923475-C-A

83646758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923475-C-T

83646816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923452-G-T

http://identifiers.org/hco/11/GRCh38#83646873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91923398-A-C

83646948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91923337-T-C

83647134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91922881-T-C

83647160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91922849-T-C

83647189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91922812-G-T

83647373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91922641-T-A

http://identifiers.org/hco/11/GRCh38#83647592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91922490-C-A

83647592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 91922490-C-T

http://identifiers.org/hco/11/GRCh38#83647655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91922428-C-A

83647835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91922267-T-C

http://identifiers.org/hco/11/GRCh38#83648121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91921990-A-C

83648331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91921750-T-C

83648441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91921642-G-T

83648445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91921638-G-T

83648695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91921436-T-C

83648928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91921082-A-T

83649219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920805-C-T

83649380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920646-T-C

83649544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920480-A-G

83649930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920153-G-A

83649933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920150-A-G

83650006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920096-C-G

83650020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91920082-G-A

83650487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91919698-T-C

83650536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91919644-G-C

83650542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91919636-G-A

83651350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917762-G-A

83651408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917722-G-A

83651501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917586-C-T

83651517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917566-G-A

83651517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917566-G-T

83651523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917560-G-A

83651523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917560-G-T

http://identifiers.org/hco/11/GRCh38#83651530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91917552-C-A

83651530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917552-C-G

83651530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917552-C-T

83651588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917495-T-C

http://identifiers.org/hco/11/GRCh38#83651715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91917371-C-A

83651715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917371-C-T

83651832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 91917259-T-C

83651859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917232-T-A

83651890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917214-G-C

http://identifiers.org/hco/11/GRCh38#83651965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91917140-C-A

83651965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91917140-C-G

http://identifiers.org/hco/11/GRCh38#83651999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91917106-C-A

83652147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916977-G-A

83652147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916977-G-T

83652315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916830-T-C

http://identifiers.org/hco/11/GRCh38#83653248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91916418-C-A

83653346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916350-G-A

83653394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916302-T-C

http://identifiers.org/hco/11/GRCh38#83653418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91916278-A-C

83653687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91916009-G-C

83654391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91915455-G-A

83654496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91915347-G-A

83654713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91915136-G-A

83654832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91915019-A-T

83654960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91914896-T-G

83655008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91914826-G-A

83655128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91914715-T-C

83655282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91914585-A-G

83655730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91914168-C-T

83655993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913934-G-A

83655993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913934-G-C

83656279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913673-G-A

83656661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913322-C-T

83656869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913113-T-C

83656917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91913069-T-C

83657007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91912979-T-C

http://identifiers.org/hco/11/GRCh38#83657397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91912609-C-A

83657492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91912534-C-T

83658325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91911870-A-G

83658522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91911672-A-G

http://identifiers.org/hco/11/GRCh38#83658621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91911573-C-A

83658621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91911573-C-T

83659559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91910906-C-G

83659578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91910887-A-G

83659651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91910816-T-C

83659691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91910785-C-G

83659921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91910529-G-A

83660243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909660-A-G

83660249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909654-T-G

83660711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909215-G-T

83660838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909064-G-A

83660868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909034-C-T

83660878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91909003-G-A

83660916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908948-T-A

http://identifiers.org/hco/11/GRCh38#83660921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91908943-A-C

83660939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908924-T-A

http://identifiers.org/hco/11/GRCh38#83660977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91908887-C-A

http://identifiers.org/hco/11/GRCh38#83660978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91908886-A-C

83661108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908759-T-C

83661123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908744-G-A

83661123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908744-G-T

83661147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908728-G-A

83661276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908596-A-T

83661724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908125-G-A

83661733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908116-A-G

83661757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91908092-G-A

83661863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91907990-T-C

83661873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91907981-G-C

http://identifiers.org/hco/11/GRCh38#83663186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91907308-C-A

83663432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91907055-T-G

83663443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91907044-G-A

http://identifiers.org/hco/11/GRCh38#83663459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91907028-C-A

83663459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91907028-C-T

http://identifiers.org/hco/11/GRCh38#83663543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91906944-C-A

83663551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91906936-A-G

83663581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91906906-C-T

83663721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91906776-T-C

83663768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91906746-T-A

http://identifiers.org/hco/11/GRCh38#83663908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91906611-C-A

83664077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91906074-T-C

83664194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91905950-G-A

83664357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91905772-G-A

83664788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91905356-A-G

83664859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91905191-T-G

83664889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91905136-T-C

83664947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904888-C-T

83665010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904826-G-T

83665027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904808-G-A

83665106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904733-G-A

83665168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904676-G-A

83665242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91904604-A-G

83665840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91903936-A-T

83665967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91903714-C-G

83666261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91903415-G-A

83666754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91903275-G-T

83666992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902965-A-G

83667214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902753-T-C

83667697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902279-A-G

83667697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902279-A-T

83667708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902270-A-G

83667858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91902102-G-A

83668134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901945-T-A

83668180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901883-C-G

83668180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901883-C-T

http://identifiers.org/hco/11/GRCh38#83668339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91901791-A-C

83668573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901526-C-T

83669274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901091-T-C

83669306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901059-A-G

83669311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91901054-A-G

83669457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900959-G-T

83669468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900948-T-G

83669571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900853-C-T

83670037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900642-A-G

83670134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900543-G-A

83670525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91900169-T-C

83671337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91897886-A-G

83671337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91897886-A-T

83673102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91894573-C-G

83673172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91894512-A-G

83673654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91894058-C-T

83673815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91893902-A-G

83674090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91893118-G-A

83674224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892849-A-G

83674272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892797-T-C

83674350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892721-T-A

83674712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892394-G-C

83674743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892363-G-T

83674758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892347-T-A

83675018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91892126-G-A

83675504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91890620-T-A

83675554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91890566-A-G

83675846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91890133-T-G

83675992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889982-G-C

83676133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889845-T-C

83676167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889812-T-C

83676791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889472-G-T

83676966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889297-G-A

83677237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889042-C-G

83677237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91889042-C-T

83677311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91888938-T-C

83677541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91888667-G-T

83677550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91888658-G-T

http://identifiers.org/hco/11/GRCh38#83677649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91888578-C-A

http://identifiers.org/hco/11/GRCh38#83677696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91888534-A-C

83677696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91888534-A-G

83678235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887965-T-A

83678983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887788-G-A

83678983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887788-G-T

83679116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887659-G-A

83679116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887659-G-C

83679120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887655-G-A

83679197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887568-C-T

83679200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887565-T-C

83679383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887389-C-G

83679383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887389-C-T

83679422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887350-T-C

83679427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91887345-G-A

83679827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91886950-G-A

83679931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91886883-G-T

http://identifiers.org/hco/11/GRCh38#83680498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91886065-A-C

83680529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91886033-C-T

83681087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885461-A-G

83681115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885434-T-C

83681239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885297-G-C

83681239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885297-G-T

83681458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885101-A-G

83681487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91885072-T-A

http://identifiers.org/hco/11/GRCh38#83682065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91884523-C-A

83682065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91884523-C-T

83682157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 91884431-C-T

http://identifiers.org/hco/11/GRCh38#83682284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91884305-C-A

83682509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91884080-G-T

http://identifiers.org/hco/11/GRCh38#83682923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91883654-C-A

83682923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883654-C-T

83682970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883594-G-T

83683001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883564-G-A

83683002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883563-C-G

83683032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883533-G-A

83683050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91883515-A-T

83683721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91882816-T-C

83683851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91882690-A-G

83683868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91882672-G-A

83683892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91882648-G-A

http://identifiers.org/hco/11/GRCh38#83684642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91874199-C-A

83684664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91874177-T-C

http://identifiers.org/hco/11/GRCh38#83684675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91874166-C-A

83684870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91873764-A-G

83684881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91873753-C-T

83684938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91873695-C-T

83686198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871875-A-G

83686323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871766-A-G

83686326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871763-T-C

83686365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871702-A-G

83686670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871455-T-C

83686714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871413-C-T

83686830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871308-T-C

83686939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871204-G-A

83687063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871110-A-G

83687239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871019-T-C

83687239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91871019-T-G

83687300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870973-A-T

83687407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870866-A-G

83687557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870721-T-G

83687745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870604-G-A

83688508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870083-A-G

83688573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91870014-T-C

83688786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91869831-T-C

83688786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91869831-T-G

83690261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91867643-T-C

83690794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91865312-G-A

83690936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91865179-C-T

83690982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91865134-A-G

83691095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91865023-G-T

83691181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864939-G-C

83691282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864853-C-T

83691431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864714-T-C

83691472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864673-C-G

83691472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864673-C-T

83691481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864664-G-C

83692117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91864060-A-G

83692824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91863137-T-C

83692909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91863047-T-C

83692926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 91863028-T-G

83692984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862969-T-C

http://identifiers.org/hco/11/GRCh38#83692997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91862952-C-A

83693143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862825-T-C

83693185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862783-A-T

83693234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862770-G-A

83693267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862737-A-T

83693295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91862709-T-C

http://identifiers.org/hco/11/GRCh38#83693944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91862020-C-A

83694080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861969-C-T

83694345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861519-A-T

83694360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861459-A-G

83694384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861429-T-C

83694384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861429-T-G

83694685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861127-G-C

83694724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91861091-G-A

http://identifiers.org/hco/11/GRCh38#83694811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91861006-A-C

83694956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91860875-G-A

83695816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91860393-G-A

83695876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91860336-G-A

83695974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91860254-C-T

83696027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91860199-T-A

83696421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859850-C-T

83696574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859701-T-C

83696632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859659-G-C

83696736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859565-A-G

83696845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859447-G-T

83696915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859370-T-G

83696999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859297-A-G

http://identifiers.org/hco/11/GRCh38#83697109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91859195-C-A

83697109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91859195-C-T

83698302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857818-G-C

83698531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857597-C-T

83698653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857477-C-T

83698807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857364-A-G

83698830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857339-G-A

http://identifiers.org/hco/11/GRCh38#83698833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91857336-A-C

83698999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91857180-C-T

83699200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91856992-T-C

83700616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91856552-G-C

83700702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91856468-G-C

83701196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855991-G-A

83701407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855797-T-C

83701448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855764-A-T

83701735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855471-G-A

83701780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855427-G-A

83701780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855427-G-T

http://identifiers.org/hco/11/GRCh38#83701822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91855388-A-C

83702193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91855046-T-C

83702263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854956-G-T

83702319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854915-A-G

83702330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854904-T-C

83702344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854890-A-G

83702444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854811-T-C

http://identifiers.org/hco/11/GRCh38#83702644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91854655-A-C

83702708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854566-C-T

83702900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854344-G-A

83702962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854283-G-A

83703037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854216-C-T

http://identifiers.org/hco/11/GRCh38#83703112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91854141-C-A

83703112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91854141-C-G

83703717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853877-T-C

83703742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853853-A-G

83703763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853832-T-C

http://identifiers.org/hco/11/GRCh38#83703784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91853813-A-C

83703813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853795-G-A

83703843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853768-A-G

83705697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91853075-T-A

83706379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91852726-G-C

http://identifiers.org/hco/11/GRCh38#83706408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91852700-C-A

83706442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91852635-A-G

83706542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91852529-A-T

http://identifiers.org/hco/11/GRCh38#83706664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91852331-A-C

83706716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91852267-G-A

83706717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91852266-C-T

83707156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91851794-T-C

83707156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91851794-T-G

83707340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91851638-T-C

http://identifiers.org/hco/11/GRCh38#83707347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91851631-A-C

83708135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91851209-T-A

http://identifiers.org/hco/11/GRCh38#83708150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91851195-A-C

83708257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91851096-T-C

http://identifiers.org/hco/11/GRCh38#83708279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91851073-C-A

http://identifiers.org/hco/11/GRCh38#83708362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91851004-A-C

83708456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91850862-G-A

http://identifiers.org/hco/11/GRCh38#83708532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91850788-C-A

83708613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91850077-T-C

83708711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91850001-A-G

83708741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849971-G-A

83708872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849886-G-C

83708873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849885-A-G

83708896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849862-C-T

http://identifiers.org/hco/11/GRCh38#83708926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91849851-C-A

83709004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849783-G-A

83709133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849686-A-G

83709549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849376-T-C

83709757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849174-G-C

83709757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849174-G-T

83709762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849169-T-G

83709780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849151-T-C

83709791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849140-C-T

83709912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849038-T-A

83709912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91849038-T-C

83711146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91847323-G-C

83711153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91847316-A-G

83711305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91847188-C-T

83711535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91846971-T-G

83711545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91846961-G-C

83713005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91846271-T-A

83713288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845974-G-A

83713492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845779-C-T

83713548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845660-T-G

http://identifiers.org/hco/11/GRCh38#83713797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91845428-A-C

83713805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845420-G-C

83713805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845420-G-T

83713952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845276-C-T

83714073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91845194-T-G

83714655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91842583-C-T

83715283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841952-A-G

83715305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841930-G-A

83715305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841930-G-T

http://identifiers.org/hco/11/GRCh38#83715345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91841903-C-A

http://identifiers.org/hco/11/GRCh38#83715480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91841793-A-C

83715576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841694-T-G

http://identifiers.org/hco/11/GRCh38#83715738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91841555-C-A

83715902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841400-C-T

83715964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841283-T-G

83716066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91841053-T-C

http://identifiers.org/hco/11/GRCh38#83716151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91840974-A-C

83716173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91840954-C-T

83716317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91840812-G-A

83716425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91840712-C-T

83716572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91839489-A-G

83716633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91839445-T-G

83716636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91839443-C-T

83716693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91839386-G-C

83716953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91839144-A-G

83717131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838961-A-G

83717168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838928-A-G

83717527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838595-A-G

83717856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838269-G-T

83717974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838152-C-T

83718040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838086-G-C

83718103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838024-G-A

83718103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91838024-G-C

83718185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91837937-T-C

83719043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91836902-T-C

83719049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91836896-G-A

83719278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91836099-A-G

http://identifiers.org/hco/11/GRCh38#83719839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91835945-C-A

83720392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91834270-C-T

83720425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91834234-G-A

83720612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91834063-G-A

83720620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91834055-C-T

83720662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91834015-T-C

http://identifiers.org/hco/11/GRCh38#83720726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91833949-C-A

83720801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833869-C-T

http://identifiers.org/hco/11/GRCh38#83720852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91833656-C-A

83720852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833656-C-T

83720913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833538-C-T

http://identifiers.org/hco/11/GRCh38#83720934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91833525-C-A

83720948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833511-G-T

83721003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833459-G-T

83721079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833369-G-T

83721452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91833020-A-G

83721771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91832208-T-C

83721851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91832132-T-C

83721886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91832105-T-C

83721893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91832097-A-T

83722021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831962-A-G

83722133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831855-T-C

http://identifiers.org/hco/11/GRCh38#83722211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91831768-A-C

83722211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831768-A-G

83722338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831633-T-G

83722504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831482-G-A

83722705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831332-A-T

83722707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831330-G-A

83722707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831330-G-T

83722763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831295-T-C

83722846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831231-T-C

http://identifiers.org/hco/11/GRCh38#83722915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91831168-C-A

83722915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831168-C-T

83722978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831094-A-G

83723016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91831056-G-T

83724016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830779-C-T

83724017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830778-T-C

83724102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830692-G-C

83724125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830658-C-T

83724176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830603-A-G

83724383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830404-T-A

83724454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830324-T-A

http://identifiers.org/hco/11/GRCh38#83724556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91830260-C-A

83724633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91830183-T-C

http://identifiers.org/hco/11/GRCh38#83724705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91830108-C-A

http://identifiers.org/hco/11/GRCh38#83724844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91829969-C-A

83724844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829969-C-G

83724936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829878-G-A

83724990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829816-T-A

83724990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829816-T-C

83725111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829698-T-C

83725111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829698-T-G

83725114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829695-T-A

83725264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829545-A-G

http://identifiers.org/hco/11/GRCh38#83725285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#91829525-C-A

83725304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829506-G-A

83725366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40179
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91829446-A-G