85855084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914941-G-T

85855114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914920-A-G

85855114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914920-A-T

85855123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914916-T-C

http://identifiers.org/hco/11/GRCh38#85855126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89914913-A-C

85855126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914913-A-G

85855131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89914908-A-G

http://identifiers.org/hco/11/GRCh38#85855142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89914897-C-A

85855161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89914880-G-A

85855161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89914880-G-T

85855172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914849-T-C

85855290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914734-T-C

85855290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914734-T-G

85855316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89914712-C-T

85855333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89914700-G-A

85855339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914694-G-A

85855339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914694-G-T

85855444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89914591-T-C

http://identifiers.org/hco/11/GRCh38#85855608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89914506-C-A

85855638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89914477-A-G

85856826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89913794-G-A

http://identifiers.org/hco/11/GRCh38#85856870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89913751-C-A

85861144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912862-G-A

85861145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912861-T-G

85861478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912372-C-T

85861538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912310-A-T

http://identifiers.org/hco/11/GRCh38#85861625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89912226-C-A

85862022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912202-G-A

85862022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89912202-G-T

85862922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89911274-T-C

85862924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89911272-T-C

85862925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89911271-G-C

85863335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89910878-T-G

85863836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89910381-G-T

http://identifiers.org/hco/11/GRCh38#85864228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89910037-C-A

85864311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89909967-T-C

85864350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89909932-T-C

85864742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89909096-T-C

85864762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89909062-T-C

85864871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908972-G-A

85864875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908968-G-A

85864927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908905-C-T

85865003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908846-G-T

http://identifiers.org/hco/11/GRCh38#85865015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89908834-A-C

85865015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908834-A-G

85865027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908823-T-A

85865027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908823-T-C

http://identifiers.org/hco/11/GRCh38#85865077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89908769-A-C

85865077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908769-A-G

85865077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908769-A-T

85865334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908539-G-T

85865350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908527-T-C

85865354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908523-A-G

85866025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908262-T-C

85866048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908239-T-G

85866278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89908047-T-G

http://identifiers.org/hco/11/GRCh38#85866370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89907957-C-A

85867565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907487-T-C

85867565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907487-T-G

85867593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907460-A-G

85867617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907442-A-G

85867654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907406-A-G

85867787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907285-T-A

85867895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907177-G-A

85867949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89907124-C-T

85868182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89906877-T-C

85868982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89903670-C-T

85869003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89903655-A-G

85869105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89903554-A-G

85869261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89903412-C-T

85869262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89903411-A-G

85869553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902843-A-T

85869803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902470-T-C

85869977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902335-C-G

85869977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902335-C-T

85870040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902294-G-A

85870114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902237-T-C

85870187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902167-T-C

85870252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89902129-G-A

85873168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89899809-A-G

http://identifiers.org/hco/11/GRCh38#85873251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89899733-C-A

85873251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89899733-C-G

85873251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 89899733-C-T

85873845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89899016-A-G

85873874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89898987-G-A

85874411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897535-G-A

http://identifiers.org/hco/11/GRCh38#85882471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89896427-C-A

85882471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896427-C-T

http://identifiers.org/hco/11/GRCh38#85882472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89896426-A-C

85882472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896426-A-G

85882488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896410-G-A

85882488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896410-G-C

85882595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89896303-C-T

85882597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89896301-G-A

85882597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89896301-G-C

85882597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89896301-G-T

85882774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896145-G-T

85882791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896128-T-C

http://identifiers.org/hco/11/GRCh38#85882796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89896123-A-C

85882796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896123-A-T

85882899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896036-A-T

85885485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894791-T-C

85885626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894634-C-T

http://identifiers.org/hco/11/GRCh38#85885721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89894544-A-C

85885726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894539-T-C

85885760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894505-T-C

85885773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894448-C-T

85885951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89894038-G-A

85886071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893922-T-A

85886094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893519-G-T

http://identifiers.org/hco/11/GRCh38#85886115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89893498-C-A

85886115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893498-C-G

85886115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893498-C-T

85886116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893497-A-G

85886140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893474-T-C

85886145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893469-A-G

http://identifiers.org/hco/11/GRCh38#85886146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89893468-C-A

85886146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893468-C-T

http://identifiers.org/hco/11/GRCh38#85886179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89893435-C-A

85886179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893435-C-T

85886223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89893387-G-A

85886223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89893387-G-C

85886298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 89893312-C-T

85886461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893148-T-C

85886472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89893137-G-A

85892326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89892624-T-C

http://identifiers.org/hco/11/GRCh38#85892395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89892544-A-C

85892860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89892081-T-A

85892860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89892081-T-C

85893170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891833-T-C

85893489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891564-A-G

85894209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891008-A-G

85894215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891002-T-C

85894383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890833-T-G

85894401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890815-C-T

85894661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890599-C-G

85894844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890308-C-T

85894970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890024-T-C

85894994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89890002-C-T

http://identifiers.org/hco/11/GRCh38#85895204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89889637-A-C

85895204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889637-A-G

85895223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889593-T-A

85895223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889593-T-C

85895240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889576-A-G

85895240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889576-A-T

85895358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89889478-G-A

85895358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89889478-G-C

85895358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89889478-G-T

85895401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889435-T-C

85895456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889381-A-G

85895457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889380-G-T

85895485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889349-G-A

85895581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889248-T-C

85895627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889181-T-C

85895663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889144-A-T

85896598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888936-A-G

85897267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888117-G-A

85897293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888096-C-T

85897476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887945-T-C

85897570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887864-C-T

85897708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887729-T-G

85897815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887371-A-G

http://identifiers.org/hco/11/GRCh38#85898197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89887223-A-C

85898970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89886129-G-A

85899051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89886053-T-G

85899052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89886052-T-C

85899861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884858-G-A

http://identifiers.org/hco/11/GRCh38#85899937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89884800-C-A

85900026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884651-G-C

85900049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884622-G-C

85900497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884236-A-T

http://identifiers.org/hco/11/GRCh38#85900507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89884226-C-A

85900512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884221-T-C

85900551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884182-A-G

http://identifiers.org/hco/11/GRCh38#85900621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89884108-A-C

85900625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884104-C-T

85902380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883502-A-G

85902485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883397-G-A

85902626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883251-T-A

85902626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883251-T-C

85902682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883190-G-C

85906460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881710-T-A

85906505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881645-T-C

85906953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881551-G-C

85906976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881530-T-C

85907751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880907-C-G

85908065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880641-C-G

http://identifiers.org/hco/11/GRCh38#85908097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89880620-A-C

85910527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879500-T-C

85910552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879480-A-G

85910552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879480-A-T

85910553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879479-T-C

85910586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879446-T-A

85910603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879429-T-C

85910672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879368-G-C

85910685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879355-A-G

85910778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879275-T-C

http://identifiers.org/hco/11/GRCh38#85911211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89879187-A-C

85911211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879187-A-T

http://identifiers.org/hco/11/GRCh38#85911259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89879140-C-A

85911315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89879084-A-G

85911323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89879076-A-G

85915323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89877731-A-G

85915323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89877731-A-T

http://identifiers.org/hco/11/GRCh38#85915373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89877684-C-A

85915459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: 89877604-C-T

http://identifiers.org/hco/11/GRCh38#85915564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89877523-C-A

85915564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877523-C-T

http://identifiers.org/hco/11/GRCh38#85915568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89877509-C-A

85915568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877509-C-G

85915568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877509-C-T

http://identifiers.org/hco/11/GRCh38#85915644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89877456-C-A

85915644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877456-C-T

85915647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877453-G-A

85915647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89877453-G-T

85916117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: 89875922-G-A

85916153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: 89875886-G-C

85916171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: 89875868-G-A

85916185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: synonymous variant
orthologous variants: 89875854-G-A

http://identifiers.org/hco/11/GRCh38#85916199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89875840-A-C

85916220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: 89875819-A-G

http://identifiers.org/hco/11/GRCh38#85916230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89875809-C-A

85916257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875782-T-C

http://identifiers.org/hco/11/GRCh38#85916357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89875685-A-C

85916363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875679-C-T

85916365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875677-A-G

85916369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875673-T-A

85916425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875634-T-A

85916425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875634-T-C

http://identifiers.org/hco/11/GRCh38#85916434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89875625-C-A

http://identifiers.org/hco/11/GRCh38#85916444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89875615-C-A

85916444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875615-C-T

85916490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875567-C-T

85916501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron variant
orthologous variants: 89875556-G-A

85916570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89875489-C-G

85916613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89875460-T-C

85916613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 89875460-T-G

85916772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875287-T-C

85916773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875286-A-G

85916773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875286-A-T

85916847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875216-A-G

85917876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874312-T-C

85917998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874233-A-G

http://identifiers.org/hco/11/GRCh38#85918319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89874012-C-A

85919056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89873556-C-T

85919227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89873398-G-A

85919227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89873398-G-T

http://identifiers.org/hco/11/GRCh38#85919248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89873376-C-A

85919270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89873355-A-T

http://identifiers.org/hco/11/GRCh38#85919284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89873341-A-C

http://identifiers.org/hco/11/GRCh38#85919602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#89873047-C-A

85919602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89873047-C-T

85919684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89872961-G-C

85919704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89872946-A-G

85919809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89872873-G-C

85919834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89872850-T-A

http://identifiers.org/hco/11/GRCh38#85919846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#89872838-C-A

85919846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89872838-C-T

85919901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89872791-A-T

85919993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89872707-G-A