3263790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182473-G-A

http://identifiers.org/hco/7/GRCh38#3263912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141182581-C-A

http://identifiers.org/hco/7/GRCh38#3263958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141182629-C-A

3263958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182629-C-T

3264050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182724-G-C

http://identifiers.org/hco/7/GRCh38#3264065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141182738-C-A

3264065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182738-C-T

3264197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182853-A-G

3264220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182876-G-A

3264220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182876-G-C

http://identifiers.org/hco/7/GRCh38#3264242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141182896-C-A

3264242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182896-C-T

3264417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141182992-T-C

3264455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141183035-G-A

3264461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141183041-T-C

3264465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141183045-A-G

3264615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141183213-A-G

3264699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183296-A-G

3264699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183296-A-T

http://identifiers.org/hco/7/GRCh38#3264746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141183343-C-A

3264746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183343-C-G

3264746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183343-C-T

3264755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183353-G-A

3264755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: non coding transcript exon variant
orthologous variants: 141183353-G-T

3264810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141183423-C-T

http://identifiers.org/hco/7/GRCh38#3265213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141183945-C-A

3265213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141183945-C-T

3265697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141185278-G-A

3265697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141185278-G-C

3265709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141185290-T-C

3265835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141185421-T-C

3266177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141185974-A-G

3267920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141188027-C-T

3267946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188052-C-G

3267946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188052-C-T

3268041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141188130-C-T

http://identifiers.org/hco/7/GRCh38#3268059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141188148-C-A

3268146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188236-T-C

3268146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188236-T-G

3268160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188250-G-A

3268377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188468-G-A

3268553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141188641-C-T

http://identifiers.org/hco/7/GRCh38#3268595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141188677-C-A

3269264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141189412-T-A

http://identifiers.org/hco/7/GRCh38#3269500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141189607-A-C

3269500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141189607-A-T

3270018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141189985-T-C

3270099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141190059-G-T

3270442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141190536-T-C

3270485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141190575-G-A

3270499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141190589-G-T

3271722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141191222-C-G

3271722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141191222-C-T

http://identifiers.org/hco/7/GRCh38#3272046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141191543-A-C

3272398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141192661-G-C

http://identifiers.org/hco/7/GRCh38#3272443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141192704-C-A

3272682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141192947-C-T

3272689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141192954-A-G

3272887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141193154-T-C

3272903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141193170-C-T

http://identifiers.org/hco/7/GRCh38#3273091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141193361-C-A

3273121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141193391-G-A

3273947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195468-C-T

3274051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195541-T-A

3274051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195541-T-C

3274131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195635-A-G

3274293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195801-A-T

3274321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195827-T-A

3274436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195946-G-A

3274436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195946-G-T

http://identifiers.org/hco/7/GRCh38#3274453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141195964-C-A

3274453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195964-C-T

3274477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141195985-G-A

3274496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141196002-G-A

3274549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141196055-T-A

3274549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141196055-T-C

3279463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141198339-G-A

3279555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141198433-A-G

3279701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141198523-A-G

3279813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141198619-G-T

3280680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141199398-C-T

3280886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201032-G-A

3281207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201392-G-C

3281219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201404-C-T

http://identifiers.org/hco/7/GRCh38#3281234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141201419-A-C

3281631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201598-T-C

3281796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201747-T-C

3281796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201747-T-G

3281913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201852-G-A

3281913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141201852-G-C

3282406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205630-T-C

3282417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205640-C-T

3282437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205660-T-A

3282483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205707-T-C

3282513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205737-G-A

3282513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205737-G-T

3282674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205897-G-A

http://identifiers.org/hco/7/GRCh38#3282711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141205922-A-C

3282736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205947-C-T

3282747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205958-T-C

3282748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141205959-G-A

3282844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206020-C-T

3283397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206156-C-G

http://identifiers.org/hco/7/GRCh38#3283433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141206178-C-A

3283445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206190-G-A

3283528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206277-G-A

3283560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206308-G-A

3283560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206308-G-T

http://identifiers.org/hco/7/GRCh38#3285796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141206668-A-C

3286018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206882-C-G

3286121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141206986-G-T

3286155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141207020-G-C

3286209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141207074-T-C

3286303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141207149-A-G

3288315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209145-A-G

http://identifiers.org/hco/7/GRCh38#3288451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141209270-A-C

3288604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209422-T-C

3288623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209546-G-T

3288637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209560-T-G

3288717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209610-A-G

3288719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209612-T-C

3288764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209654-A-G

3288793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209683-A-G

3288851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209748-T-G

3288924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209814-T-C

3288924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141209814-T-G

3290588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141213994-T-G

3290684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214090-G-A

3290694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214100-G-T

3290709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214115-T-G

3290877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214298-C-T

http://identifiers.org/hco/7/GRCh38#3291002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141214383-C-A

3291002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214383-C-T

3291633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214900-G-A

3291633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214900-G-T

3291707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141214978-A-G

3294791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141220154-G-A

3294791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141220154-G-T

3294948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141220325-A-T

http://identifiers.org/hco/7/GRCh38#3295279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141220623-A-C

3295279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141220623-A-G

3295596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141221882-G-A

3295596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141221882-G-T

http://identifiers.org/hco/7/GRCh38#3296843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141222921-C-A

3296843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141222921-C-G

3297010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141223060-T-C

3297977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141224444-G-T

3298214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141224984-T-C

3298663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141225080-G-A

3299119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141225553-T-C

3299878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141225908-G-A

3299905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141225949-A-G

3300155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226184-C-T

3300278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226310-C-T

3300370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226409-T-A

3300370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226409-T-C

3300384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226422-C-G

3300578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226623-C-T

3300703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141226727-G-T

3300820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141226870-C-G

3300908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141226975-G-C

3300908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141226975-G-T

3301028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227116-G-A

3301028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227116-G-C

3301029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227117-C-G

3301152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227222-G-T

3301248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227312-G-A

http://identifiers.org/hco/7/GRCh38#3301339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227408-C-A

3301339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227408-C-T

http://identifiers.org/hco/7/GRCh38#3301347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227416-C-A

3301347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227416-C-T

http://identifiers.org/hco/7/GRCh38#3301388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227476-C-A

3301388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227476-C-G

3301388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227476-C-T

3301391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227480-G-A

3301391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227480-G-T

3301437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227505-A-G

3301687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227695-G-A

http://identifiers.org/hco/7/GRCh38#3301747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227734-C-A

3301747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227734-C-G

3301747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227734-C-T

http://identifiers.org/hco/7/GRCh38#3301771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227749-C-A

3301771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227749-C-G

3301771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227749-C-T

3301805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227771-G-A

3301805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141227771-G-T

http://identifiers.org/hco/7/GRCh38#3301902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141227865-C-A

3301902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227865-C-G

3301902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227865-C-T

3301903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227866-G-A

3301903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227866-G-C

3301903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141227866-G-T

3302099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141229312-G-A

3302099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141229312-G-T

3302244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229464-G-A

3302244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229464-G-C

3302244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229464-G-T

3302294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229515-G-A

3302294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229515-G-T

http://identifiers.org/hco/7/GRCh38#3302324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141229545-C-A

3302324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229545-C-G

3302324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229545-C-T

3302417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229612-G-A

http://identifiers.org/hco/7/GRCh38#3302445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#141229640-C-A

3302445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229640-C-G

http://identifiers.org/hco/7/GRCh38#3302470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141229664-C-A

3302470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141229664-C-T

http://identifiers.org/hco/7/GRCh38#3302474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#141229668-C-A

3302474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141229668-C-T

3302618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229799-T-A

3302618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229799-T-C

3302618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141229799-T-G

3303046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40883
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141230219-C-T