http://identifiers.org/hco/11/GRCh38#86374771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89552828-C-A

http://identifiers.org/hco/11/GRCh38#86374776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89552819-C-A

http://identifiers.org/hco/11/GRCh38#86374793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89552801-C-A

http://identifiers.org/hco/11/GRCh38#86374814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89552780-C-A

86374814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89552780-C-G

86374814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89552780-C-T

86374891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89552719-G-A

86374891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89552719-G-C

86374891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89552719-G-T

86374936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552673-G-A

86374936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552673-G-T

86374956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552653-G-A

86374956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552653-G-T

86374973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552636-T-A

86374973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552636-T-C

86374973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552636-T-G

86375042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89552590-A-T

86375199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 89552431-G-C

86375227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89552403-T-G

http://identifiers.org/hco/11/GRCh38#86375260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89552372-C-A

86375280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89552362-T-C

86375297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89552345-G-T

86375384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89552241-T-C

86375384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89552241-T-G

86383815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549926-A-G

86383925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549849-T-C

86384018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549753-T-C

86384060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549711-C-G

86384313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549183-G-A

86384313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549183-G-C

86384405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89549020-C-T

86384558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548861-C-G

86384628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548796-G-A

86384628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548796-G-T

86384659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548738-T-C

86384839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548549-G-T

86385681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89548026-G-C

86385798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547898-G-A

http://identifiers.org/hco/11/GRCh38#86385950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89547569-C-A

86385950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547569-C-T

86385959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547560-T-C

86385984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547408-G-A

86385984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547408-G-T

86385992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547359-A-G

86385992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547359-A-T

86385993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547358-T-C

86386017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547334-A-G

86386017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547334-A-T

86386019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547332-T-C

86386019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547332-T-G

http://identifiers.org/hco/11/GRCh38#86386092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89547264-C-A

86386092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89547264-C-G

86386092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89547264-C-T

86386152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547232-T-A

86386152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547232-T-C

86386152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547232-T-G

86386285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547130-G-T

86386380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547040-T-C

86386385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89547035-C-T

http://identifiers.org/hco/11/GRCh38#86386521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89546876-C-A

86386744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546653-C-T

http://identifiers.org/hco/11/GRCh38#86386849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89546549-C-A

86386849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546549-C-T

86386885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546513-G-A

86386950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546447-G-A

86386950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546447-G-T

86387007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546392-G-C

86387025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546368-C-T

86387191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546262-A-G

86387393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546187-G-A

86387393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546187-G-C

86387396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546184-A-T

86387416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546164-T-C

86387418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89546162-A-G

86387552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89546023-A-G

86387552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89546023-A-T

86387642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89545933-G-A

http://identifiers.org/hco/11/GRCh38#86387701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89545874-C-A

86387704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545871-G-A

86387704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545871-G-T

http://identifiers.org/hco/11/GRCh38#86387717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89545858-C-A

86387748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545827-G-A

86387748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545827-G-T

http://identifiers.org/hco/11/GRCh38#86387758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89545820-C-A

http://identifiers.org/hco/11/GRCh38#86387794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89545784-C-A

86387794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89545784-C-G

86387930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545535-C-T

86388129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545338-A-G

86388224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545260-C-T

86388287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89545225-T-G

86388352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89545158-T-C

86388432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545083-C-T

86388491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89545029-A-G

86388562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544862-T-G

http://identifiers.org/hco/11/GRCh38#86388887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89544573-A-C

86388920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544540-T-G

86390302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544261-A-G

86390328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544230-A-G

86390469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544113-T-C

86390555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544036-G-A

86390555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89544036-G-T

86390740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543898-G-T

86390775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543876-C-T

86390819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543866-A-G

86390946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543738-G-A

86391056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543601-G-A

86391056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543601-G-T

86391522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543096-C-G

86391605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543027-G-T

86391610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89543022-T-C

86392396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89542710-T-G

86392421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89542692-A-G

86392570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89542545-G-T

86392591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89542524-C-T

86392609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89542506-G-A

86392678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89542437-T-C

86392705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89542410-A-G

86392815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89542304-T-C

86393152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89541884-T-A

86393355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89541650-G-A

86393572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89541333-T-C

86393790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89541001-G-A

86393918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540900-G-T

86394054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540773-A-G

86394189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540663-C-G

86394308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540557-T-C

86394405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540472-T-G

86394467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540422-A-G

86394528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540359-T-C

86394572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540323-C-G

86394731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89540171-A-G

http://identifiers.org/hco/11/GRCh38#86395018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89539957-C-A

86395018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539957-C-G

86395018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539957-C-T

http://identifiers.org/hco/11/GRCh38#86395055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89539920-A-C

86395124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539850-A-G

http://identifiers.org/hco/11/GRCh38#86395210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89539784-C-A

86395210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539784-C-G

86395210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539784-C-T

86395222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539772-A-G

86395243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539762-T-C

86395323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 89539687-C-T

86395377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539634-T-C

86395377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539634-T-G

86395397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89539614-G-A

86395429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539582-C-T

86395499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539500-T-C

86395546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539444-T-A

86395546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539444-T-C

http://identifiers.org/hco/11/GRCh38#86396249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89539039-C-A

86396281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89539007-A-T

86396351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89538938-T-A

86396438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89538454-T-C

86396591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89538337-C-T

86396609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89538297-C-T

http://identifiers.org/hco/11/GRCh38#86397035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89537551-C-A

http://identifiers.org/hco/11/GRCh38#86397090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89537497-A-C

86397118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537471-T-A

86397345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537281-A-G

86397511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537118-G-A

86397511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537118-G-T

http://identifiers.org/hco/11/GRCh38#86397564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89537066-C-A

86397589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537041-T-C

86397603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89537027-A-G

86397652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89536978-C-T

http://identifiers.org/hco/11/GRCh38#86397729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89536901-A-C

86397729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89536901-A-T

86397760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536870-G-C

86397760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536870-G-T

86397770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536860-T-C

86397770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536860-T-G

86397795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536835-A-G

86397796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536834-G-A

86397799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89536831-A-G

86400904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89535254-G-A

86400930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89535228-A-G

86406975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89532569-C-G

86407184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89532367-T-C

86407474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89532033-T-C

http://identifiers.org/hco/11/GRCh38#86407476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89532031-C-A

86407575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89531627-T-C

http://identifiers.org/hco/11/GRCh38#86407627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89531575-A-C

86407627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89531575-A-G

http://identifiers.org/hco/11/GRCh38#86408003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89531193-C-A

86408020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89531086-A-G

86408026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89531078-G-T

http://identifiers.org/hco/11/GRCh38#86408077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89531019-C-A

86408166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89530927-T-A

86408166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89530927-T-C

86408208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89530882-G-A

86408416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89530644-T-C

86409126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529752-T-C

86409265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89529434-A-G

86409345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89529354-A-G

http://identifiers.org/hco/11/GRCh38#86409354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89529345-C-A

86409393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529306-A-G

86409401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529298-G-A

86409401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529298-G-C

86409401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529298-G-T

http://identifiers.org/hco/11/GRCh38#86409402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89529297-C-A

86409402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529297-C-G

86409402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529297-C-T

86409473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89529172-G-A

86409986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89528647-C-T

http://identifiers.org/hco/11/GRCh38#86410041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89528604-C-A

86410208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89528442-C-T

86410225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89528425-T-C

http://identifiers.org/hco/11/GRCh38#86410414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89528237-C-A

86410414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89528237-C-T

86410509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89528152-A-G

86410816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527836-T-C

86411187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527513-C-T

86411231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527451-G-A

86411253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527401-C-T

86411302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527347-G-A

http://identifiers.org/hco/11/GRCh38#86411337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89527310-A-C

86411493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527180-A-G

86411633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527036-T-C

86411672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89527001-A-T

86412349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89526820-T-C

86412349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89526820-T-G

86412350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89526819-A-G

86413615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89526372-T-C

86413638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89526348-T-C

86413680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89526304-G-A

86413690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89526294-T-C

http://identifiers.org/hco/11/GRCh38#86413788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89526208-C-A

86413897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525951-C-T

86413912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525936-G-A

86413914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525934-G-A

86414021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525837-T-C

86414041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525817-T-C

86414121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525733-A-G

86414213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron variant
orthologous variants: 89525654-T-C

86414745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89525441-G-T

86414764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89525402-A-G

86414838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 89525324-C-T

86414928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89525231-T-C

86414928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89525231-T-G

86415035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89525124-G-A

86415175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89525019-T-C

86415175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89525019-T-G

86415326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89524868-C-G

86415326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89524868-C-T

86415354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89524817-C-T

86415355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89524809-T-C

86415679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89524515-T-G

http://identifiers.org/hco/11/GRCh38#86419216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89519762-C-A

86419216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519762-C-G

86419413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519575-T-C

86419494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519499-C-G

86419544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519314-T-G

86419691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519185-A-T

http://identifiers.org/hco/11/GRCh38#86419785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89519101-C-A

86419785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89519101-C-T

86419940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89518940-C-T

http://identifiers.org/hco/11/GRCh38#86420167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89518483-C-A

86420204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89518448-T-C

86420878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89516873-C-T

86420968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89516776-G-C

86421195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89516555-A-G

86422439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515980-G-T

86422442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515977-G-A

86422442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515977-G-C

86422442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515977-G-T

86422520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515910-G-T

http://identifiers.org/hco/11/GRCh38#86422561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89515865-C-A

86422561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89515865-C-T

86422646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89515780-C-T

86422653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89515773-G-A

86422653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89515773-G-T

86422740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515685-C-T

86422772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515663-G-T

http://identifiers.org/hco/11/GRCh38#86422893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89515539-C-A

86422904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515528-T-G

86422963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515483-G-A

86422963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515483-G-T

86422970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515476-G-C

86422970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515476-G-T

http://identifiers.org/hco/11/GRCh38#86423000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89515446-C-A

86423000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515446-C-T

86423006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515440-G-T

http://identifiers.org/hco/11/GRCh38#86423031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89515420-C-A

86423031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515420-C-T

86423073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515386-G-A

86423073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 89515386-G-T

86423107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26281
most severe consequence: 3 prime UTR variant
orthologous variants: 89515355-T-C