82078461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698033-G-A

82078461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698033-G-T

82078466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698038-T-C

http://identifiers.org/hco/17/GRCh38#82078532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120698077-C-A

82078532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698077-C-G

82078532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698077-C-T

http://identifiers.org/hco/17/GRCh38#82078688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120698244-C-A

82078688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698244-C-T

82078792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698333-G-A

82078792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698333-G-T

82078916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698451-G-C

82078916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698451-G-T

82078972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698495-C-G

82078972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3 prime UTR variant
orthologous variants: 120698495-C-T

82079035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120698568-G-A

82079035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120698568-G-T

82079139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120698658-G-A

82079139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120698658-G-C

82079272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120698809-G-A

82079323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120698871-C-T

82079417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120698961-C-T

82079429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120698973-G-A

82079429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120698973-G-T

82079522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699066-C-T

http://identifiers.org/hco/17/GRCh38#82079570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120699114-C-A

82079570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699114-C-T

82080160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120699348-T-C

82080206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699394-C-T

82080320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120699511-G-T

82080403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699578-G-A

82080403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120699578-G-T

82080427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699602-G-A

82080427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699602-G-T

82080510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699685-G-A

82080510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699685-G-T

82080517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699692-G-A

82080517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699692-G-C

82080517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699692-G-T

http://identifiers.org/hco/17/GRCh38#82080532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120699707-C-A

82080532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120699707-C-T

82080597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120699772-T-C

82080598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120699773-G-A

82080598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 120699773-G-T

82080628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699800-G-A

82080628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699800-G-C

82080628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699800-G-T

82080654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699818-G-A

82080654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699818-G-C

82080654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699818-G-T

82080658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699822-T-C

82080677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699841-A-G

82080677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120699841-A-T

82080723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120699882-G-A

82080723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 120699882-G-T

http://identifiers.org/hco/17/GRCh38#82080729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120699888-C-A

82080729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 120699888-C-T

82080753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120699912-G-A

82080753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120699912-G-T

82080756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120699915-G-A

82080756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120699915-G-C

82080756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120699915-G-T

http://identifiers.org/hco/17/GRCh38#82080793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120699952-C-A

82080793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120699952-C-T

http://identifiers.org/hco/17/GRCh38#82080978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700121-C-A

82080978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700121-C-T

82080979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700122-G-A

82080979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700122-G-T

82081088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700212-G-A

82081088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700212-G-T

http://identifiers.org/hco/17/GRCh38#82081225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700313-C-A

82081225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120700313-C-G

82081225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120700313-C-T

82081317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120700405-A-G

82081317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120700405-A-T

http://identifiers.org/hco/17/GRCh38#82081338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700426-C-A

82081338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120700426-C-G

82081338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120700426-C-T

http://identifiers.org/hco/17/GRCh38#82081365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700451-C-A

82081365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700451-C-G

82081365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700451-C-T

82081400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700488-G-A

82081400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700488-G-T

http://identifiers.org/hco/17/GRCh38#82081576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700608-C-A

82081576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700608-C-T

82081595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120700624-G-T

http://identifiers.org/hco/17/GRCh38#82082025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120700972-C-A

82082025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120700972-C-T

82082173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701120-G-A

82082173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701120-G-C

82082173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701120-G-T

82082304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701256-A-G

http://identifiers.org/hco/17/GRCh38#82082507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120701451-C-A

82082507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701451-C-T

82082611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120701551-G-A

82082681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120701621-G-T

82082692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701632-G-A

82082692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701632-G-C

82082692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701632-G-T

82082709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701645-G-A

82082709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701645-G-T

82082751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120701659-T-G

82082918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120701742-C-T

http://identifiers.org/hco/17/GRCh38#82083107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120701931-C-A

82083107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120701931-C-T

http://identifiers.org/hco/17/GRCh38#82083165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120701994-C-A

82083177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702096-G-A

82083177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702096-G-T

82083313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120702228-G-A

82083331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120702246-C-G

82083331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120702246-C-T

82083497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702406-C-G

82083497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702406-C-T

82083590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120702499-G-A

82083758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702647-T-C

82083758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702647-T-G

82083925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702812-G-A

82083925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702812-G-C

82083925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120702812-G-T

82084073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120702963-G-A

82084073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120702963-G-C

82084073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120702963-G-T

82084208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703087-C-T

82084226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120703118-A-G

82084326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120703218-G-A

82084326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120703218-G-T

http://identifiers.org/hco/17/GRCh38#82084398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120703301-C-A

82084398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703301-C-T

http://identifiers.org/hco/17/GRCh38#82084430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120703379-C-A

82084430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703379-C-T

82084457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703409-G-A

82084474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703426-C-G

82084474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703426-C-T

82084481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703433-A-G

http://identifiers.org/hco/17/GRCh38#82084489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120703443-C-A

82084489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120703443-C-T

82084577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120703548-G-A

http://identifiers.org/hco/17/GRCh38#82084604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120703575-A-C

82084619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120703590-G-A

82084694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120703665-T-A

http://identifiers.org/hco/17/GRCh38#82084742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120703718-C-A

82085203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120704195-G-A

82085203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120704195-G-T

82085313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120704307-G-C

82085389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120704383-C-T

http://identifiers.org/hco/17/GRCh38#82085430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120704429-C-A

82085430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120704429-C-G

82085448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120704446-G-A

82085448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120704446-G-T

82085458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120704456-T-C

82085500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120704498-G-A

82085500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120704498-G-T

82085736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120704731-G-A

82085736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120704731-G-T

82085785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120704780-G-A

82085785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120704780-G-C

82085785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120704780-G-T

82085833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120704828-T-C

82085833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120704828-T-G

82085953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120704954-T-A

http://identifiers.org/hco/17/GRCh38#82085976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120704989-C-A

82085976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120704989-C-T

http://identifiers.org/hco/17/GRCh38#82086000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120705019-C-A

82086053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120705073-C-T

82086326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120705375-G-A

82086326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120705375-G-T

82086468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120705517-G-A

82086549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120705580-T-C

http://identifiers.org/hco/17/GRCh38#82086551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120705582-C-A

82086551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120705582-C-T

82086688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120705682-G-A

82086688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120705682-G-C

82086688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120705682-G-T

82087203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120705991-C-T

http://identifiers.org/hco/17/GRCh38#82087282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120706077-A-C

82087284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706079-A-G

82087299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706096-C-T

82087401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120706193-G-A

82087401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120706193-G-T

82087410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120706202-C-T

82087576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706344-C-T

82087583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706351-C-T

82087701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120706453-C-T

82087808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120706563-T-C

82087821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120706576-G-A

82088068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706826-G-C

http://identifiers.org/hco/17/GRCh38#82088086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120706843-C-A

82088086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120706843-C-T

82088176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: stop gained
orthologous variants: 120706926-G-A

82088176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120706926-G-C

82088258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120707008-G-A

82088258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120707008-G-C

http://identifiers.org/hco/17/GRCh38#82088369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120707112-A-C

82088370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707113-C-T

82088609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707348-G-C

82088673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707387-G-C

82088673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707387-G-T

82088752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707439-G-C

82088908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707603-G-A

82088928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707619-T-A

82088928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707619-T-C

82088937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707628-C-T

http://identifiers.org/hco/17/GRCh38#82088959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120707657-C-A

82088981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120707685-G-A

82088981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120707685-G-T

82089146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120707850-T-C

82089153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120707857-G-A

82089211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707909-C-T

82089223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707926-C-T

82089225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120707928-C-T

http://identifiers.org/hco/17/GRCh38#82089563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120708231-C-A

82089563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708231-C-T

82089691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120708358-G-A

82090073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120708581-C-T

82090216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708664-C-T

82090224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708672-T-G

82090292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708712-G-A

82090292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708712-G-C

82090292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708712-G-T

http://identifiers.org/hco/17/GRCh38#82090340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120708760-C-A

82090340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708760-C-G

82090353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708789-G-A

82090353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708789-G-T

82090355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708791-G-A

82090355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120708791-G-T

82090514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120708951-G-A

82090514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120708951-G-T

http://identifiers.org/hco/17/GRCh38#82090670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709088-C-A

82090670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709088-C-T

http://identifiers.org/hco/17/GRCh38#82090754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709145-C-A

82090754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709145-C-T

http://identifiers.org/hco/17/GRCh38#82090757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709148-C-A

82090757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709148-C-T

82090849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709223-G-C

http://identifiers.org/hco/17/GRCh38#82090857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709238-C-A

82090857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709238-C-T

82090931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709308-C-G

82090931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709308-C-T

82090993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709370-G-A

82091011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709388-T-G

82091020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709397-G-A

82091020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709397-G-T

82091073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120709450-T-A

82091132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709450-T-C

82091202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709543-G-C

82091202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120709543-G-T

http://identifiers.org/hco/17/GRCh38#82091241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709583-C-A

82091241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709583-C-G

82091241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709583-C-T

http://identifiers.org/hco/17/GRCh38#82091270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709612-C-A

82091270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709612-C-T

82091439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709781-C-T

82091457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709799-G-A

http://identifiers.org/hco/17/GRCh38#82091471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120709813-C-A

82091471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709813-C-G

82091471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120709813-C-T

82091547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709889-G-A

82091553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120709895-G-A

http://identifiers.org/hco/17/GRCh38#82091667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710009-C-A

82091667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120710009-C-T

82091710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710052-A-G

http://identifiers.org/hco/17/GRCh38#82091760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710093-C-A

82091760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710093-C-G

82091760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710093-C-T

82091783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710116-G-A

82091783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710116-G-T

82091833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710160-T-C

82091872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710197-C-T

82092190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710434-T-C

82092219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710447-C-T

http://identifiers.org/hco/17/GRCh38#82092312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710509-C-A

82092312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710509-C-T

82092374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710566-A-G

82092379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710571-A-G

82092379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710571-A-T

http://identifiers.org/hco/17/GRCh38#82092424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710602-C-A

82092424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710602-C-G

82092424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710602-C-T

http://identifiers.org/hco/17/GRCh38#82092622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710796-C-A

82092622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710796-C-T

82092668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710837-G-C

82092668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120710837-G-T

http://identifiers.org/hco/17/GRCh38#82092781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710939-C-A

82092781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120710939-C-G

82092781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120710939-C-T

http://identifiers.org/hco/17/GRCh38#82092803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120710961-A-C

http://identifiers.org/hco/17/GRCh38#82092857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711017-C-A

82092857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711017-C-T

82092928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711102-G-A

82092928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711102-G-C

82092988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711162-C-T

82093028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711203-A-G

http://identifiers.org/hco/17/GRCh38#82093247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711386-C-A

82093247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711386-C-T

http://identifiers.org/hco/17/GRCh38#82093301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711440-C-A

82093301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711440-C-T

82093331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711470-A-G

http://identifiers.org/hco/17/GRCh38#82093340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711479-C-A

82093340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711479-C-T

82093346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120711485-G-A

82093346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: missense variant
orthologous variants: 120711485-G-C

82093487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711599-C-T

82093493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711605-G-A

82093493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711605-G-C

82093557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711657-T-C

82093580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711705-A-G

82093585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711710-G-A

82093591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120711718-G-A

http://identifiers.org/hco/17/GRCh38#82093812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711904-C-A

82093812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711904-C-T

82093890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711941-G-A

82093890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711941-G-T

http://identifiers.org/hco/17/GRCh38#82093972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120711957-C-A

82093972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711957-C-G

82093972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120711957-C-T

82094197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712123-A-G

82094197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712123-A-T

82095119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712605-C-T

82095281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712789-A-G

http://identifiers.org/hco/17/GRCh38#82095304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120712884-C-A

82095304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712884-C-T

82095305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712885-G-A

82095305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712885-G-C

82095305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712885-G-T

82095309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120712889-G-A

82095313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120712897-G-A

82095363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120712947-C-T

82095393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: synonymous variant
orthologous variants: 120712977-G-A

82095616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120713135-T-G

82095640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120713150-C-G

http://identifiers.org/hco/17/GRCh38#82096238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120713508-C-A

82096238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron variant
orthologous variants: 120713508-C-T

http://identifiers.org/hco/17/GRCh38#82096501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120713719-C-A

82096501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120713719-C-T

http://identifiers.org/hco/17/GRCh38#82096506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120713724-C-A

82096506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120713724-C-T

82096995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714072-G-A

82096995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714072-G-C

82096995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714072-G-T

http://identifiers.org/hco/17/GRCh38#82096996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714073-C-A

82096996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714073-C-T

82097014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714091-T-A

82097014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714091-T-C

82097023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714100-G-A

82097023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714100-G-C

82097023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714100-G-T

82097126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714207-C-T

http://identifiers.org/hco/17/GRCh38#82097147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714229-C-A

82097147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714229-C-T

http://identifiers.org/hco/17/GRCh38#82097184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714266-A-C

82097184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714266-A-G

http://identifiers.org/hco/17/GRCh38#82097302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714375-C-A

82097302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120714375-C-T

http://identifiers.org/hco/17/GRCh38#82097308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714381-A-C

82097328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714398-C-G

82097392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120714455-G-A

82097484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120714510-T-C

82097514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120714529-G-A

82097514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120714529-G-T

82097597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120714576-G-A

82097597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120714576-G-T

82097650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714609-A-G

82097811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120714762-G-A

http://identifiers.org/hco/17/GRCh38#82098052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#120714826-C-A

82098052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120714826-C-T