86547151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144680739-T-C

86547151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 144680739-T-G

86548710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680599-T-A

86548710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680599-T-G

86548720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680589-T-C

86548724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680585-G-T

86548728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680581-G-T

86548771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680535-T-C

86548818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680487-G-A

86548854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680438-T-A

86548897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680388-A-G

86548974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680310-T-C

86549015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680251-T-C

http://identifiers.org/hco/1/GRCh38#86549030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144680236-C-A

86549053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680214-C-G

86549101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680164-T-C

86549212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680053-C-T

86549214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680051-C-T

86549234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144680028-A-T

86549291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144680004-G-C

86549458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679849-T-A

86549605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679719-T-C

86549652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679684-T-C

86549807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679520-G-A

86549810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679517-C-T

86549859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679486-G-T

86549891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679449-G-T

86550004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679308-G-A

86550030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679283-C-T

86550327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144679068-G-A

86550405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144678987-G-A

86559539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676906-G-A

86559664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676786-C-G

86559667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676783-A-G

86559742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676705-T-C

86559747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676700-G-A

86559747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676700-G-T

86559821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676629-G-A

86559845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676609-T-A

http://identifiers.org/hco/1/GRCh38#86559873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144676570-C-A

86559873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676570-C-T

86559878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676565-A-G

86559878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676565-A-T

86560032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144676411-A-G

86560080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 144676363-T-C

86560082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676361-G-A

http://identifiers.org/hco/1/GRCh38#86560122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144676314-A-C

86560133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676302-A-G

86560144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676288-G-A

86560301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144676134-A-G

86560328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144676107-G-A

86560391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676050-T-A

86560423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676019-A-G

86560430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676012-A-G

86560431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676011-G-A

86560431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144676011-G-T

86560445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675999-A-G

86560459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675985-A-G

86560505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675945-G-A

86560505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675945-G-T

86563370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675678-C-G

86563552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675515-G-A

86563552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675515-G-T

86563711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144675122-G-A

86563717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144675116-A-G

http://identifiers.org/hco/1/GRCh38#86563738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144675095-C-A

86563738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144675095-C-G

86563738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144675095-C-T

86563759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 144675074-G-A

86563759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 144675074-G-T

http://identifiers.org/hco/1/GRCh38#86563813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144675016-C-A

86563813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675016-C-T

86563822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675007-T-C

86563823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144675006-T-G

86563888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674936-A-G

86563888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674936-A-T

86563904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674919-T-A

86563904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674919-T-G

86563921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674902-G-T

86564799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674624-C-T

86564954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674486-T-A

86564971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674469-C-G

86565021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674405-A-G

86565204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674226-G-C

86565204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674226-G-T

86565220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674215-C-T

86565223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144674212-T-C

86565356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144674086-T-G

86565364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144674078-A-G

86565419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144674023-G-A

86565443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144673999-A-G

86565510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144673929-T-G

http://identifiers.org/hco/1/GRCh38#86565519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144673844-C-A

86565538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144673824-A-T

86565820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144672179-G-A

86565820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 144672179-G-T

http://identifiers.org/hco/1/GRCh38#86565867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#144672132-C-A

86565867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144672132-C-T

http://identifiers.org/hco/1/GRCh38#86565897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144672102-C-A

86565897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144672102-C-G

86565913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144672086-A-G

86565913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 144672086-A-T

86566041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144671934-T-C

http://identifiers.org/hco/1/GRCh38#86566147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144671833-C-A

86566147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144671833-C-T

86566163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144671816-T-A

86566164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144671815-G-T

86566251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144671749-A-G

86566684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144670209-T-C

86566734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144670160-G-C

86566879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144670052-G-C

http://identifiers.org/hco/1/GRCh38#86566883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144670049-A-C

86566975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669984-G-A

86567150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669842-A-G

86567320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669689-T-A

86567342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669668-A-G

http://identifiers.org/hco/1/GRCh38#86567391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144669620-C-A

86567391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669620-C-T

86567407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669605-T-C

http://identifiers.org/hco/1/GRCh38#86567433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144669578-C-A

86567433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144669578-C-T

http://identifiers.org/hco/1/GRCh38#86567547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144669464-A-C

86567606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144669405-T-C

86567611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144669400-G-A

86567626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144669385-G-A

86567769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669250-G-T

86567778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144669241-T-A

86570672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144668142-T-C

86570761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144668072-T-C

86570928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667914-G-T

86570956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667885-G-T

http://identifiers.org/hco/1/GRCh38#86570972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667872-C-A

86570972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667872-C-G

86570972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667872-C-T

86570982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667865-T-C

86570982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667865-T-G

86571015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667838-C-T

86571018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667835-A-G

86571018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667835-A-T

http://identifiers.org/hco/1/GRCh38#86571026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667827-A-C

86571026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667827-A-G

86571026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667827-A-T

http://identifiers.org/hco/1/GRCh38#86571043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667813-C-A

86571055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667801-G-A

86571055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667801-G-T

86571082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144667774-T-C

http://identifiers.org/hco/1/GRCh38#86571093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667763-A-C

86571096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144667760-C-T

86571182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 144667674-G-A

86571211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144667645-A-G

86571226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 144667630-A-G

86571260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667596-A-G

86571260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667596-A-T

86571291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667565-T-C

http://identifiers.org/hco/1/GRCh38#86571300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667556-A-C

http://identifiers.org/hco/1/GRCh38#86571301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667555-A-C

86571352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667508-A-T

86571356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667504-A-G

86571369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667474-G-A

86571369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667474-G-C

86571369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667474-G-T

http://identifiers.org/hco/1/GRCh38#86571373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667470-C-A

86571376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667467-T-A

86571376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667467-T-C

86571394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144667449-T-C

http://identifiers.org/hco/1/GRCh38#86571409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667434-C-A

86571409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 144667434-C-T

86571425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667417-A-G

http://identifiers.org/hco/1/GRCh38#86571427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144667415-C-A

86571427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667415-C-T

86571473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667373-G-A

86571482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667367-A-G

86571484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667365-A-G

86571544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667300-G-T

86571551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667293-A-G

86571556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667288-T-C

86571557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667287-G-T

86571569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667275-G-T

86571572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667272-T-G

86571582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667262-G-T

86571795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667195-A-G

86571813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667178-G-A

86571856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667138-C-T

86571880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667114-A-G

86571884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144667110-T-C

http://identifiers.org/hco/1/GRCh38#86572129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666883-A-C

86572325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666772-G-A

86572378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666719-C-T

86572380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666717-T-G

86572414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666683-T-C

86572436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666661-T-G

86572442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666655-T-C

86572466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666627-G-T

http://identifiers.org/hco/1/GRCh38#86572509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666590-C-A

86572523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666576-A-G

86572525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666574-G-T

http://identifiers.org/hco/1/GRCh38#86572559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666540-A-C

86572564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666535-T-C

http://identifiers.org/hco/1/GRCh38#86572570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666526-C-A

86572570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144666526-C-T

http://identifiers.org/hco/1/GRCh38#86572698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666398-A-C

http://identifiers.org/hco/1/GRCh38#86572718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666378-C-A

86572718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 144666378-C-T

86572724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144666372-A-G

86572724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144666372-A-T

86572741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144666353-G-A

86572741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144666353-G-C

http://identifiers.org/hco/1/GRCh38#86572762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144666332-C-A

86573883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144665428-T-C

http://identifiers.org/hco/1/GRCh38#86574084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144665222-A-C

86574377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144664180-A-G

86574412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144664145-G-T

http://identifiers.org/hco/1/GRCh38#86574417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144664140-C-A

86574606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663900-A-T

http://identifiers.org/hco/1/GRCh38#86574614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144663892-A-C

86574649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663857-T-G

http://identifiers.org/hco/1/GRCh38#86574785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144663717-A-C

86574842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663665-G-A

86574842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663665-G-C

86574848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663659-T-C

86574944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663561-G-A

86575091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663427-C-T

86575195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663324-C-T

http://identifiers.org/hco/1/GRCh38#86575214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144663300-C-A

86575272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663233-T-A

86575272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663233-T-C

86575287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663202-T-A

86575287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663202-T-C

86575294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663195-A-G

86575310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144663179-A-G

86575336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663152-G-A

http://identifiers.org/hco/1/GRCh38#86575353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144663135-C-A

86575365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663123-G-A

86575386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663102-A-G

86575395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663093-A-G

86575401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144663087-C-G

86575401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 144663087-C-T

86575491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144662997-G-A

86575491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144662997-G-T

86575539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144662949-G-C

86575590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144662898-A-G

86575618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662870-T-C

http://identifiers.org/hco/1/GRCh38#86575626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144662862-C-A

86575626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662862-C-G

86575626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662862-C-T

http://identifiers.org/hco/1/GRCh38#86575643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144662843-C-A

86575643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662843-C-T

86576555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662416-C-T

http://identifiers.org/hco/1/GRCh38#86576651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144662294-C-A

86576764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662174-C-G

86576953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144662010-C-T

86577084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661907-A-G

86577097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661894-A-G

http://identifiers.org/hco/1/GRCh38#86577130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144661863-C-A

86577173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661827-T-A

http://identifiers.org/hco/1/GRCh38#86577175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144661825-C-A

86577253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661740-A-T

86577287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661674-G-C

86577295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661666-A-G

86577329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661610-C-T

http://identifiers.org/hco/1/GRCh38#86577469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144661285-A-C

86577701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661067-A-G

86577705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661062-A-G

86577720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144661047-G-A

86577802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660969-A-T

http://identifiers.org/hco/1/GRCh38#86577805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144660966-C-A

86577805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660966-C-T

86577808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660963-A-T

86577865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660909-T-C

86577882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660887-T-C

86577952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144660813-T-C

86577988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144660777-G-A

86578009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144660756-G-A

86578077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660688-G-A

86578077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660688-G-C

86578145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660615-A-G

86578146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660614-A-G

86578146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660614-A-T

86578883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660364-G-A

86578959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660295-A-G

86578997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660257-A-G

86579075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144660180-T-C

86579204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659876-G-A

86579204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659876-G-T

http://identifiers.org/hco/1/GRCh38#86579246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144659837-C-A

86579246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659837-C-T

86579248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659835-G-T

86579276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659804-A-G

http://identifiers.org/hco/1/GRCh38#86579408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144659670-C-A

86579431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659647-G-T

86579449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659629-G-A

86579449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659629-G-T

86579450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659628-T-C

86579458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659620-C-G

86579458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 144659620-C-T

http://identifiers.org/hco/1/GRCh38#86579466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144659612-A-C

86579483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659595-A-G

86579484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 144659594-C-T

http://identifiers.org/hco/1/GRCh38#86579485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144659593-C-A

86579524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144659554-G-C

86579604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659474-A-G

86579604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659474-A-T

86579628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659450-G-A

86579628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659450-G-T

http://identifiers.org/hco/1/GRCh38#86579641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144659436-A-C

86579660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659423-G-C

86579660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659423-G-T

86579661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659422-G-A

86579661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659422-G-T

86579716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144659339-T-C

86579834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658945-G-A

86579862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658928-A-T

86579877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658913-T-C

86579902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658887-T-C

http://identifiers.org/hco/1/GRCh38#86579904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144658885-C-A

86579904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658885-C-T

86579905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658884-T-C

86579919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 144658870-T-G

86579950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144658841-T-C

86580100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144658691-A-T

86580113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144658678-T-A

86580337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144658490-A-G

http://identifiers.org/hco/1/GRCh38#86580648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#144658214-C-A

86580648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2018
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 144658214-C-T