http://identifiers.org/hco/2/GRCh38#3703718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28602323-C-A

3703718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28602323-C-T

3703730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28602315-G-T

3703933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28602119-G-A

3703933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 28602119-G-T

3707229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28600992-A-T

3707769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28599800-G-C

http://identifiers.org/hco/2/GRCh38#3707964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28599603-C-A

3708194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598147-G-A

3708199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598142-A-G

3708205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28598136-G-A

3708444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597363-G-T

3708463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597344-G-A

3708463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597344-G-C

3708463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597344-G-T

3708491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597316-G-T

http://identifiers.org/hco/2/GRCh38#3708510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28597297-C-A

3708510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28597297-C-T

3723913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593682-A-G

3723928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593667-C-G

http://identifiers.org/hco/2/GRCh38#3723940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28593666-C-A

http://identifiers.org/hco/2/GRCh38#3723941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28593665-C-A

3724258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593427-T-C

3724300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593392-C-T

3724302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593390-T-G

3724587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593174-A-G

3724657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593106-G-A

3724708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593061-A-G

3724821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28593004-G-A

3724927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592923-G-A

3725036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592851-G-A

3725983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592461-G-A

3725983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592461-G-C

3725983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592461-G-T

3725992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28592452-G-T

http://identifiers.org/hco/2/GRCh38#3726025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28592433-C-A

3726025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28592433-C-T

3726043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592415-G-A

3726043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592415-G-T

3726046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592412-G-T

3726211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28592267-T-A

3726596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591934-A-G

3726804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591726-C-T

http://identifiers.org/hco/2/GRCh38#3726854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28591669-A-C

3726854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591669-A-G

3726854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591669-A-T

3726874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591649-T-C

3726874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591649-T-G

3726939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591608-G-A

3726957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591590-T-C

3726967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591580-G-T

3727009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28591539-C-T

3727018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28591530-C-T

http://identifiers.org/hco/2/GRCh38#3727069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28591479-C-A

3727069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 28591479-C-T

3727091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591457-A-G

http://identifiers.org/hco/2/GRCh38#3727161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28591388-C-A

3727162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591387-T-C

http://identifiers.org/hco/2/GRCh38#3727191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28591368-C-A

3727191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591368-C-T

http://identifiers.org/hco/2/GRCh38#3727195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28591364-C-A

3727195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591364-C-T

3727342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591269-C-G

3727342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28591269-C-T

3728447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28590215-C-T

3728449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28590213-T-C

3728494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28590167-C-G

3728515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28590146-G-A

3728873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28589864-G-T

http://identifiers.org/hco/2/GRCh38#3728880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28589857-C-A

3729200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28589603-C-T

3737022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28587334-G-C

3737069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28587296-T-C

3741144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28586296-C-T

3741789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585715-T-A

3741789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585715-T-C

3741789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585715-T-G

3741812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585692-G-T

3741873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585624-C-G

3741873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28585624-C-T

3741915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28585582-T-A

3741945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28585552-A-G

3742081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28585421-G-A

3750871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28582808-C-T

3750965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28582726-C-T

http://identifiers.org/hco/2/GRCh38#3751394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28582104-C-A

3751431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28582052-G-A

3751593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28581889-T-C

3751654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28581824-A-G

3751681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28581786-T-A

3751895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28581652-T-C

3752597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28580633-T-C

3752597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28580633-T-G

http://identifiers.org/hco/2/GRCh38#3752693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28580546-C-A

3752853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 28580394-A-G

3752916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28580331-A-G

3754571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28578679-T-C

http://identifiers.org/hco/2/GRCh38#3754659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28578596-A-C

3754660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28578595-G-C

3767293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28577168-G-A

3767293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28577168-G-T

3767422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28577047-G-A

3767695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 28576857-T-C

3767903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28576667-T-C

3767903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28576667-T-G

3767907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28576663-G-T

http://identifiers.org/hco/2/GRCh38#3768021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28575683-C-A

3768021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575683-C-G

3768061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575644-A-T

3768071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575634-T-C

3768123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575585-T-C

3768177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575535-G-A

http://identifiers.org/hco/2/GRCh38#3768194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28575525-A-C

3768194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575525-A-T

3768379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575361-C-T

3768381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575359-G-C

3768469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575266-G-T

3768474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28575256-G-A

http://identifiers.org/hco/2/GRCh38#3769109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28575000-C-A

3769109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28575000-C-G

3769109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28575000-C-T

http://identifiers.org/hco/2/GRCh38#3769164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574944-C-A

3769164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574944-C-T

http://identifiers.org/hco/2/GRCh38#3769168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574940-C-A

3769168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574940-C-G

3769168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574940-C-T

http://identifiers.org/hco/2/GRCh38#3769196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574912-C-A

3769196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574912-C-T

http://identifiers.org/hco/2/GRCh38#3769217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574865-C-A

3769217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574865-C-T

3769219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574863-G-A

3769219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574863-G-T

3769220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574862-G-A

3769220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574862-G-T

http://identifiers.org/hco/2/GRCh38#3769253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574827-C-A

3769253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574827-C-T

3769276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574805-G-A

3769276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574805-G-C

3769349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28574734-A-G

3769361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 28574722-C-T

3769453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574637-T-C

3769461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574629-G-T

3769469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574621-C-G

3769477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574613-G-A

3769477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574613-G-C

3769477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574613-G-T

3769486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574606-T-C

3769534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574559-T-A

http://identifiers.org/hco/2/GRCh38#3769536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574557-C-A

3769536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574557-C-T

http://identifiers.org/hco/2/GRCh38#3769541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28574553-A-C

3769541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574553-A-G

3769541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574553-A-T

3769688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574436-T-C

3769708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574416-C-T

3769897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574261-G-A

3769950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574220-G-A

3770029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574090-G-A

3770035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28574044-G-A

http://identifiers.org/hco/2/GRCh38#3770341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28573640-A-C

3770450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28573554-T-G

3770504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28573502-A-T

3770541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28573465-A-G

3770553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28573456-C-T

3771145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28572228-G-T

3771417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28571927-G-A

3773949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28570138-G-A

3774342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569771-C-T

3774380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569734-C-T

http://identifiers.org/hco/2/GRCh38#3774416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28569697-C-A

3774419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569694-G-A

3774427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569686-G-A

3774557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569577-T-C

3774658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28569469-G-A

3778346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28567827-G-C

3778356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28567817-C-T

3778395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28567778-T-A

3778444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28567727-A-G

3778469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28567703-T-A

3778704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566820-A-G

3778704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566820-A-T

http://identifiers.org/hco/2/GRCh38#3778775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28566755-C-A

3778775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566755-C-T

http://identifiers.org/hco/2/GRCh38#3778777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28566753-C-A

3778782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566748-G-A

3778785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566745-G-C

3778785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566745-G-T

3778789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566741-A-G

3778795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566733-T-C

3778795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566733-T-G

3778800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566728-T-G

3778801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566727-G-A

3778809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28566719-T-A

3778810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 28566718-C-T

3778876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28566652-G-A

3778940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566582-G-A

3778940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566582-G-T

3779025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566508-G-A

3779025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566508-G-C

3779051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566487-A-G

3779051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566487-A-T

3779121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28566425-C-T

3779713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565953-A-G

3779746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28565917-G-A

3779746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28565917-G-T

3779767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565899-G-A

3779823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565850-G-T

3779830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565843-G-A

3780183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565575-A-G

3780454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28565340-G-C

3780923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28564900-A-G

3781075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28564754-G-T

3781089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28564740-A-G

3781454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28564404-C-G

3782252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563977-G-C

3782325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563924-T-C

3782734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563525-C-G

3782886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563364-G-A

http://identifiers.org/hco/2/GRCh38#3782971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28563288-C-A

3783068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563202-A-G

3783145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563128-A-G

3783172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563096-A-G

3783249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563025-T-A

3783249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28563025-T-C

3783274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562993-T-A

3783278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562989-C-T

3783448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562831-T-C

3783515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562774-C-T

3783616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562709-C-T

3784101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562275-T-C

3784177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28562203-G-T

3784833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561262-A-T

3784886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561176-G-A

http://identifiers.org/hco/2/GRCh38#3784909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28561153-C-A

3784909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561153-C-T

3784931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561131-C-G

3784956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561109-T-A

3784956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561109-T-C

3784962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561103-T-C

3785001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561064-T-A

3785001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561064-T-C

3785048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28561015-T-C

http://identifiers.org/hco/2/GRCh38#3785087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28560976-A-C

3785124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560944-T-C

3785137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560931-T-C

3785177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560900-C-T

3785218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560860-G-A

http://identifiers.org/hco/2/GRCh38#3785230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28560850-C-A

3785230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560850-C-T

3785257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560824-A-T

3785626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560608-C-G

3785849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560406-G-A

3786019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28560265-G-T

3787018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28559913-A-G

3787960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28558432-T-C

3788073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28558317-C-T

3788075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28558315-G-T

3788149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28558251-G-C

3788418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 28558018-G-T

3788449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28557988-G-A

3788610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28557829-A-G

3788619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28557820-C-T

3788698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28557775-G-A

3789469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28557028-G-C

3790350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28556243-G-A

3790590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555991-T-C

3790638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555943-T-C

3790773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555809-G-A

3791212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555676-A-G

3791212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555676-A-T

3791265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28555649-T-A

http://identifiers.org/hco/2/GRCh38#3791754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28555235-C-A

3792226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28554808-A-G

3792311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28554759-G-T

3792349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28554723-G-A

3792642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28553871-G-T

3792702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28553812-C-T

3793146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28553393-C-T

3793810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28552219-G-A

3793825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28552204-G-T

3793842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28552187-C-T

http://identifiers.org/hco/2/GRCh38#3801800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28549973-C-A

3801937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28549884-A-T

http://identifiers.org/hco/2/GRCh38#3801946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28549875-C-A

3802031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28549780-G-C

3802544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28549153-C-T

http://identifiers.org/hco/2/GRCh38#3802760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28548925-A-C

3802763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548923-A-G

3803002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548727-A-G

3803394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548421-C-G

3803394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548421-C-T

3803508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548281-A-T

3803587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548194-T-A

3803681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548108-A-G

3803707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548099-C-T

3803726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548080-C-T

3803743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28548060-C-G

3804185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28547796-G-A

3804453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28547279-C-T

3805556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28546767-A-G

3805650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28546673-C-T

3824899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28536219-A-G

3825105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28536071-C-T

3825334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28535840-G-A

3825356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28535818-T-A

3825786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28535444-A-G

3825928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28535329-T-G

3825930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28535327-T-G

3826641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28534520-T-A

3827054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28534204-C-G

3827161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28534088-G-A

3827168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28534081-A-G

3827313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533927-A-G

3827313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533927-A-T

http://identifiers.org/hco/2/GRCh38#3827317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28533923-A-C

3827317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533923-A-T

3827536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533700-T-C

3827846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533455-A-G

http://identifiers.org/hco/2/GRCh38#3827848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28533453-C-A

3827848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533453-C-G

3827848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533453-C-T

3827925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533363-A-T

3827993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28533313-A-G

http://identifiers.org/hco/2/GRCh38#3828414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28532983-C-A

3828432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532965-G-A

3828480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532919-C-T

3828560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532841-C-T

3828635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532767-G-A

3828647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532756-C-T

3828673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532730-G-A

3828749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532658-A-G

3828882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532557-G-A

3828887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532552-T-C

3829028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532417-C-T

3829232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532271-A-G

3829430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532105-G-A

3829430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532105-G-C

3829492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28532045-C-T

http://identifiers.org/hco/2/GRCh38#3829556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28532000-C-A

3829677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28531890-A-G

3829921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28531656-T-G

3830193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28531212-A-G

3830281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28531120-T-C

3830508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28530876-G-A

3830746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28530510-G-T

3830771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28530487-C-T

3832006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28529355-T-C

3832089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28529272-C-G

3832089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28529272-C-T

3832373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28529010-G-A

3832384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528999-A-G

3832510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528877-C-T

3832805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528640-A-G

3832836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528609-C-T

http://identifiers.org/hco/2/GRCh38#3832864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28528582-A-C

3832942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528528-T-C

3832961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528510-G-A

3833154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528349-C-G

3833170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528333-G-A

3833170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528333-G-C

3833238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528277-C-G

3833357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28528156-A-G

3834640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28527412-A-G

3835079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28527009-T-C

3839312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28526201-A-G

3839408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28526106-A-T

3839709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28525270-G-A

3839717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28525262-C-G

3839889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28525116-A-T

3839998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28525025-C-T

3840073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28524972-A-G

3840380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524701-A-T

3840414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524662-G-A

3840428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524655-G-A

http://identifiers.org/hco/2/GRCh38#3840571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28524334-A-C

3840661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524248-A-G

3840663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524246-T-C

3840696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524222-T-G

3840801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524112-G-A

3840848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524064-G-A

3840875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28524037-G-T

3841209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28523723-G-A

3841209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28523723-G-C

3841400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28523528-A-G

3841419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28523500-A-G

3841422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28523497-A-G

http://identifiers.org/hco/2/GRCh38#3841910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28522830-A-C

3841926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522809-C-T

3842105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522648-T-A

3842131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522623-G-A

3842269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522498-A-G

3842455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522332-G-T

3842620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522174-G-A

3842683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522121-C-T

3842788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28522016-T-C

3842833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521974-G-A

http://identifiers.org/hco/2/GRCh38#3842842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28521965-C-A

http://identifiers.org/hco/2/GRCh38#3842867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28521937-C-A

3842867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521937-C-T

3842884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521920-G-C

3842885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521919-A-G

3842894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521910-G-A

3843199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521677-G-A

3843272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521619-A-G

http://identifiers.org/hco/2/GRCh38#3843273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28521618-A-C

3843567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521367-G-T

3843574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521359-T-C

3843611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521314-T-C

http://identifiers.org/hco/2/GRCh38#3843626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28521302-A-C

3843801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521149-T-C

3843851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28521102-G-C

3843991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron variant
orthologous variants: 28520940-T-C

3844076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 28520875-G-T

3844094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_lost
orthologous variants: 28520857-G-T

http://identifiers.org/hco/2/GRCh38#3844180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28520768-A-C

3844180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28520768-A-G

http://identifiers.org/hco/2/GRCh38#3844194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28520733-A-C

3844194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520733-A-G

3844242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520589-T-C

http://identifiers.org/hco/2/GRCh38#3844255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28520576-C-A

http://identifiers.org/hco/2/GRCh38#3844290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28520541-C-A

3844290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520541-C-T

3844339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520492-G-A

3844339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520492-G-T

3844402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520261-G-T

3844447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520159-A-T

http://identifiers.org/hco/2/GRCh38#3844480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28520127-C-A

3844480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520127-C-T

3844557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520049-T-G

3844579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28520024-A-G

3844757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28519851-A-T

3844852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28519761-A-T

3844894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28519720-A-G

3844907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28519706-T-C

3845566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518729-C-G

3845566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518729-C-T

3845774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518566-G-T

3845781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518559-A-G

3845852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518492-C-G

3846577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518275-G-T

3846584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518268-G-T

3846791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518076-G-T

3846823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518061-G-C

3846823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518061-G-T

3846854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518032-G-A

3846854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28518032-G-T

http://identifiers.org/hco/2/GRCh38#3847014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#28517893-C-A

3847014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32696
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28517893-C-T