http://identifiers.org/hco/4/GRCh38#105552705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132940635-C-A

105552705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132940635-C-T

105552763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132940585-A-G

105552922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132940426-A-G

http://identifiers.org/hco/4/GRCh38#105552997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132940348-A-C

105553134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132940220-A-T

105553213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132940065-G-T

http://identifiers.org/hco/4/GRCh38#105553429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132939855-C-A

105553429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939855-C-T

105553467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939814-A-G

105553507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939775-T-C

105553559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939724-T-C

105553669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939616-A-G

105553788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939513-T-A

105553804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939497-A-G

105553972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939333-T-G

105554031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939273-A-G

105554621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939102-G-A

105554621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132939102-G-C

105554889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938804-A-G

105554958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938741-A-G

105554982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938711-A-G

105555381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938368-G-A

105555381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938368-G-C

105555436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132938311-T-C

105555887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937885-T-C

105555930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937837-T-C

105556058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937726-C-T

105556461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937460-T-A

http://identifiers.org/hco/4/GRCh38#105556690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132937269-A-C

105556690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937269-A-T

105556704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937257-G-C

105556759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937203-G-A

105556762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937200-C-G

105556938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132937025-T-A

http://identifiers.org/hco/4/GRCh38#105556982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132936985-A-C

105557063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936904-T-C

105557092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936875-T-A

105557099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936868-G-A

http://identifiers.org/hco/4/GRCh38#105557151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132936835-A-C

105557196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936806-T-C

105557261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936744-T-C

105557292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936720-G-A

105557327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936687-G-A

105557327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936687-G-C

105557391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936655-A-T

105557393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936653-G-T

http://identifiers.org/hco/4/GRCh38#105557507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132936556-A-C

105557509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936554-T-A

105557568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936495-G-A

105557568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936495-G-T

105557579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936485-G-A

105557634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936443-C-T

105557713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936378-T-C

105557719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936372-G-A

105557757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936348-G-A

105557757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936348-G-T

http://identifiers.org/hco/4/GRCh38#105557767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132936338-C-A

105557767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936338-C-G

105557767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936338-C-T

105558023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936090-T-C

105558090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132936012-G-A

105558138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935972-G-A

105558215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935896-C-T

105558581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935567-T-C

105558637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935496-A-G

105558869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935259-G-A

105558869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935259-G-T

105558907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935222-G-C

http://identifiers.org/hco/4/GRCh38#105558919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132935210-C-A

105558919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935210-C-G

105558919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935210-C-T

105558948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132935196-G-T

105559268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934400-A-G

105559314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934366-G-A

105559339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934341-A-G

105559471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934215-G-T

105563983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934174-T-C

105564101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934061-T-A

105564101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132934061-T-C

http://identifiers.org/hco/4/GRCh38#105564168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132933986-C-A

105564253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132933899-G-T

105564256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132933896-T-C

105564655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132933537-A-G

105564700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132933497-A-G

105565041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929943-C-T

105565099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929885-G-T

105565156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929829-G-A

http://identifiers.org/hco/4/GRCh38#105565422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132929572-C-A

105565522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929430-G-C

105565522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929430-G-T

105565532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132929420-A-G

http://identifiers.org/hco/4/GRCh38#105565811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132928940-C-A

105565866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132928887-A-G

105566027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132928742-T-G

105566092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132928679-T-C

105566122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132928649-C-T

105569125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132926980-C-T

105569716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132926400-T-C

105569716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132926400-T-G

105571651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132924752-A-G

105571718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132924685-G-A

105571887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132924516-A-G

105572134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132924270-G-T

105572361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132923996-C-T

105572456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132923824-T-C

105572703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132923412-C-T

105572723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132923393-C-T

105572957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132922968-T-C

105573238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132922730-C-T

105573331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132922645-A-G

105573369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132922607-T-C

105583260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920292-A-G

105583324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920234-T-C

105583400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920167-G-A

105583449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920126-C-G

http://identifiers.org/hco/4/GRCh38#105583451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132920124-C-A

105583451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920124-C-T

105583499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132920077-C-T

105583946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132919651-T-C

105584050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132919555-A-T

105584279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918958-A-G

105584541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918702-A-G

105584558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918685-G-T

105584781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918545-C-T

105584958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918364-A-T

105585092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132918251-T-A

http://identifiers.org/hco/4/GRCh38#105586504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132915621-C-A

105586555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915569-T-C

105586569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915555-G-T

105586618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915511-G-C

105586874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915337-A-G

105586876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915335-G-A

105586876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915335-G-C

http://identifiers.org/hco/4/GRCh38#105586920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132915285-A-C

105586920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915285-A-T

105586972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132915238-T-C

105587759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132914281-C-T

105587766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132914274-G-A

105588167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132913932-T-C

105588222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132913883-C-T

105588385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132913717-A-G

105588615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132913466-T-A

105589017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132913092-C-T

105589109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912992-T-C

105589110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912991-A-G

105589110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912991-A-T

105589161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912942-A-T

105589280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132912807-G-A

105589318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132912769-G-A

105589318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132912769-G-C

105589442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132912645-A-G

105589571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912513-G-C

105589571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132912513-G-T

105590475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132910981-T-C

105590687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132910729-G-C

105590861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132910518-C-G

105590861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132910518-C-T

105591041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132910355-T-C

105593958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132909661-C-T

105594364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132909303-G-T

105594408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132909260-A-T

105594409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132909259-T-A

105594409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132909259-T-C

105594419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132909249-A-G

105594529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132909099-A-G

http://identifiers.org/hco/4/GRCh38#105594616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132909029-A-C

105594654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132908992-G-A

105594969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132908743-A-G

105595058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132908642-T-C

105595162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132908548-C-G

105595180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132908530-T-C

105597001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132907273-T-C

105597225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132907058-A-G

105597254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132907014-C-T

http://identifiers.org/hco/4/GRCh38#105597601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132906689-A-C

105597666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132906625-T-A

105597761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132905115-A-G

105597761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132905115-A-T

105597795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132905082-A-G

105597922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904958-A-G

http://identifiers.org/hco/4/GRCh38#105597952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132904932-A-C

105598012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904877-T-A

105598359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904664-T-G

105598460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904556-T-A

105598500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904516-G-A

http://identifiers.org/hco/4/GRCh38#105598644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132904370-C-A

105598692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904288-G-C

105598692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904288-G-T

http://identifiers.org/hco/4/GRCh38#105598707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132904276-C-A

http://identifiers.org/hco/4/GRCh38#105598737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132904250-A-C

105598760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132904228-A-G

105598877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132903146-T-C

105598938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132903095-A-G

105598970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132903066-G-A

105599120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902919-T-G

105599123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902916-G-A

105599144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902896-G-T

105599331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902742-A-G

105599384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902690-G-A

105599463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902612-C-T

105599471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902604-G-A

105599483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132902589-C-T

105599784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

105600074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

105600074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

105600110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

105600231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

http://identifiers.org/hco/4/GRCh38#105600256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

105600256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

105600260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

105600313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

105600442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

105600552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

105605225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895558-A-G

105605549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895310-A-T

105605790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895074-T-C

105605802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895062-T-C

105605814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895050-A-G

105605861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132895011-T-C

105605898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132894985-G-A

105605969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132894921-A-G

105606447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132894481-T-C

105607025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132893598-C-T

105607231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132893383-G-A

http://identifiers.org/hco/4/GRCh38#105608911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132887308-C-A

105608922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132887297-G-A

105608922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132887297-G-C

105609315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132886900-T-A

105610676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132885945-A-G

105610676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132885945-A-T

105611171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132885482-T-C

105611615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132885178-T-C

105611678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132885115-A-G

105611966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132884403-G-A

105611984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132884385-A-G

105612036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132884332-T-A

105612475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132883306-T-G

105612663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132883141-T-G

http://identifiers.org/hco/4/GRCh38#105613189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132882462-A-C

105613267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882367-A-G

105613279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882355-A-G

105613279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882355-A-T

105613326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882325-G-A

105613335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882316-T-C

105613335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882316-T-G

105613489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132882148-C-T

http://identifiers.org/hco/4/GRCh38#105613526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132882111-C-A

105613526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132882111-C-T

105613643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881994-T-A

105613643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881994-T-C

http://identifiers.org/hco/4/GRCh38#105613657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132881980-C-A

105613657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881980-C-T

105613723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881914-A-G

105613783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881860-T-A

105613783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881860-T-C

105613792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881851-A-G

105613843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881808-T-G

105613903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881746-T-G

105613995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881671-C-T

http://identifiers.org/hco/4/GRCh38#105614117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132881568-A-C

105614344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881372-T-C

105614413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881216-C-T

105614453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132881135-G-C

105614863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132880311-C-T

105614899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132880275-G-T

105619224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132876626-G-A

105619541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132876337-A-G

105619563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132876316-T-C

105619626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132876262-T-C

105619633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132876255-A-T

105619753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875924-G-A

105620070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875620-G-A

105620257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875385-A-G

105620276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875362-A-G

105620429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875223-G-A

105620506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875158-A-G

105620506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875158-A-T

105620516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132875148-C-T

105620783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874890-A-G

105620950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874741-T-A

105622068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874299-G-A

105622068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874299-G-T

105622081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874286-G-A

105622206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874168-G-A

105622371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132874026-C-T

105622468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132873941-C-G

105622835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132873563-T-C

105622839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132873559-T-C

105623130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132873188-G-A

105623144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132873177-T-C

105623644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132872392-G-A

105623644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132872392-G-T

105623686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132872350-G-C

http://identifiers.org/hco/4/GRCh38#105623755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132872291-A-C

105623847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132872218-T-C

105623901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132872163-C-T

105624555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132871232-G-A

105624677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132871116-T-C

105624777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132871024-G-A

105624816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132870987-G-T

http://identifiers.org/hco/4/GRCh38#105625179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132870430-C-A

105625179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132870430-C-T

105625342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132870310-G-C

105625395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132870255-G-A

105627231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869745-T-C

105627476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869486-C-T

105627499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869466-T-A

105627581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869346-C-T

105627660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869265-C-T

105627730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132869196-T-G

105627974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868961-C-G

105628035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868905-A-T

105628046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868894-T-A

105628212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868748-T-C

105628431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868527-T-C

105628443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868515-G-C

105628595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132868363-C-G

105629493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132867840-T-C

105629531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132867814-A-T

http://identifiers.org/hco/4/GRCh38#105629682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132867684-A-C

105629700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132867667-T-C

http://identifiers.org/hco/4/GRCh38#105629728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132867638-C-A

105629728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132867638-C-G

105629728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132867638-C-T

http://identifiers.org/hco/4/GRCh38#105629922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132867437-C-A

105630655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132866852-T-A

http://identifiers.org/hco/4/GRCh38#105630839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132866685-C-A

http://identifiers.org/hco/4/GRCh38#105630850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132866672-C-A

105630850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132866672-C-T

105631057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866465-T-A

105631057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866465-T-C

105631118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866406-A-T

105631127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866397-C-T

http://identifiers.org/hco/4/GRCh38#105631228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132866308-C-A

105631228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866308-C-T

105631268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866265-G-A

105631268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866265-G-C

105631268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866265-G-T

105631384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132866162-A-G

105631582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132865988-A-G

105631612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132865948-A-G

105631620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132865940-A-G

105631727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865846-T-A

http://identifiers.org/hco/4/GRCh38#105631738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132865835-A-C

105631738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865835-A-G

105631739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865834-T-G

105631744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865829-G-A

105631759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865814-G-C

105631791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865783-A-T

105631862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132865720-C-G

http://identifiers.org/hco/4/GRCh38#105632620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132864965-C-A

http://identifiers.org/hco/4/GRCh38#105632681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132864913-C-A

105632739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132864851-C-T

105632797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132864811-T-C

105632882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132864735-A-G

http://identifiers.org/hco/4/GRCh38#105632917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#132864705-C-A

105632924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132864698-T-C

http://identifiers.org/hco/4/GRCh38#105632943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132864680-C-A

105632950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132864673-C-T

105633046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132864580-T-C

http://identifiers.org/hco/4/GRCh38#105633072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132864555-C-A

105633072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132864555-C-T

105633132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132864495-G-C

105633575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132864059-A-G

http://identifiers.org/hco/4/GRCh38#105633888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132863775-A-C

105633912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132863751-A-G

105634126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132863533-T-C

105634349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132863294-C-T

105634566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132863078-G-A

105634852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132862806-G-A

105635486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132862029-T-C

105635486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132862029-T-G

http://identifiers.org/hco/4/GRCh38#105635487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132862028-A-C

http://identifiers.org/hco/4/GRCh38#105636018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132861603-C-A

105636128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132861343-C-T

105636227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132861240-A-G

105636282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132860036-G-A

105636282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132860036-G-T

105636299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132860019-T-A

http://identifiers.org/hco/4/GRCh38#105636338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132859983-A-C

105636338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859983-A-G

105636338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859983-A-T

105636339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859982-T-C

http://identifiers.org/hco/4/GRCh38#105636352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132859970-C-A

105636352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859970-C-T

http://identifiers.org/hco/4/GRCh38#105636363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132859955-C-A

105636363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859955-C-T

105636377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132859941-T-C

105641297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132858401-C-T

105641395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132858303-A-G

105641511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132858200-T-A

105641566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132858154-T-A

http://identifiers.org/hco/4/GRCh38#105641707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132858029-C-A

105641708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132858028-T-C

105641798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132857963-G-T

105642585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132857222-C-T

105642922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132857007-T-C

105643003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856968-A-G

105643052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856922-T-G

105643087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856895-T-C

105643107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856875-G-A

105643138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856862-T-G

105643208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856824-C-T

105643338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856710-T-C

105643442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856633-A-T

105643448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856627-G-T

105643495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856582-T-C

105643785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856281-T-C

105644299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132856078-C-T

105644409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855980-A-G

105644498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855895-G-A

105644498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855895-G-C

105644519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855874-A-T

105644590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855818-T-C

105644722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855712-T-C

105644722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855712-T-G

105644906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855519-A-T

105645094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855444-A-G

105645094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855444-A-T

http://identifiers.org/hco/4/GRCh38#105645163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132855434-C-A

105645288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132855309-C-T

http://identifiers.org/hco/4/GRCh38#105645292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132855305-C-A

http://identifiers.org/hco/4/GRCh38#105645399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132855198-C-A

105645399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855198-C-T

http://identifiers.org/hco/4/GRCh38#105645421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132855176-A-C

105645421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855176-A-G

105645504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855096-T-G

105645506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855094-T-C

http://identifiers.org/hco/4/GRCh38#105645510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132855090-A-C

105645510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132855090-A-G

105645608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132854990-G-A

105645714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132854903-A-G

105645910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132854729-T-C

105646215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132854153-T-G

http://identifiers.org/hco/4/GRCh38#105648183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132852746-C-A

105648183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852746-C-T

105648184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852745-G-A

105648188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852741-G-A

105648302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852571-T-A

105648332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852532-G-A

105648384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852476-C-T

105648396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852465-G-T

105648404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852455-G-A

105648404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852455-G-T

http://identifiers.org/hco/4/GRCh38#105648480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132852381-A-C

105648498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852364-A-G

105648521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852344-G-A

105648535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852326-T-G

105648578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132852283-G-A

105648776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852067-T-C

105648776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852067-T-G

105648777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852066-A-G

105648785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132852061-T-A

105648951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851963-A-T

http://identifiers.org/hco/4/GRCh38#105649186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132851742-C-A

105649186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851742-C-T

105649210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851717-C-T

105649283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851648-T-C

105649315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851612-A-G

105649411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851515-T-C

105649463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851463-C-G

105650719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851365-C-T

105650786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851307-A-G

105650824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851270-G-C

105651108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132851011-T-A

105651160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132850958-T-C

105651395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132850723-A-G

105651799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132850445-C-T

http://identifiers.org/hco/4/GRCh38#105652174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132850064-A-C

105652268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849977-A-G

105652461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849784-T-G

105652749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849528-G-A

105652755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849522-C-T

105653027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849259-C-T

105653030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849256-T-C

105653181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132849123-T-C

http://identifiers.org/hco/4/GRCh38#105653202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132849103-A-C

105653881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848259-C-T

105653894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848243-G-A

105653894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848243-G-T

105653912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848225-G-T

105653947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848193-A-T

105653987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848151-T-C

http://identifiers.org/hco/4/GRCh38#105653992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132848146-C-A

105653992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848146-C-T

105654033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848086-G-C

105654033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848086-G-T

105654048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848067-T-C

105654048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848067-T-G

105654055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132848060-T-C

105654146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132847969-T-C

105654146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132847969-T-G

105654178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847937-G-A

http://identifiers.org/hco/4/GRCh38#105654199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132847924-C-A

105654199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847924-C-G

105654201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847922-A-G

105654201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847922-A-T

105654229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847906-T-A

105654229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847906-T-C

http://identifiers.org/hco/4/GRCh38#105654232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132847903-C-A

http://identifiers.org/hco/4/GRCh38#105654294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132847844-A-C

105654294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847844-A-G

105654299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847839-A-G

http://identifiers.org/hco/4/GRCh38#105654469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132847686-C-A

105654713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847410-T-C

105654753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132847371-A-G

105655404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846799-A-G

105655533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846716-A-G

105655538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846711-T-C

105655543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846706-T-C

http://identifiers.org/hco/4/GRCh38#105655563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132846682-C-A

105655563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846682-C-T

http://identifiers.org/hco/4/GRCh38#105655612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132846639-C-A

105655612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132846639-C-T

105655641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132846610-T-C

105655641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132846610-T-G

105655663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132846591-G-T

105655666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132846588-G-A

105655666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132846588-G-T

105655750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846504-G-A

105656044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846167-T-C

105656395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132846080-A-T

105656586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845868-T-A

105656638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 132845828-T-C

http://identifiers.org/hco/4/GRCh38#105656791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132845686-C-A

105656791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845686-C-T

http://identifiers.org/hco/4/GRCh38#105656821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132845644-C-A

105656821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845644-C-T

105656861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845606-G-A

105656861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845606-G-C

105656861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845606-G-T

105656907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845560-G-A

105656907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132845560-G-T

105657330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844741-G-C

105657500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844588-T-A

105657578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844512-T-A

105657600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844487-T-A

105657600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844487-T-C

105657630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844455-G-A

105657925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844161-C-T

105657962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132844137-A-G

105658092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132843983-G-A

105658101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132843978-G-A

105658573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132843774-G-A

105658573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132843774-G-T

105659091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 132843299-C-G

105659091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132843299-C-T

105659174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 132843216-C-T

http://identifiers.org/hco/4/GRCh38#105659252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132843138-C-A

105659362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132843028-G-A

105659362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132843028-G-T

105662928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132842796-C-T

105665919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839738-T-A

105666029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839637-A-G

http://identifiers.org/hco/4/GRCh38#105666084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132839583-C-A

105666116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839550-T-G

http://identifiers.org/hco/4/GRCh38#105666122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132839544-C-A

105666122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839544-C-T

105666160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839513-A-G

105666212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132839462-G-C

105666288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132839386-A-T

105666297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132839377-A-G

105666409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839273-T-A

http://identifiers.org/hco/4/GRCh38#105666410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132839272-C-A

http://identifiers.org/hco/4/GRCh38#105666424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132839265-C-A

105666424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839265-C-T

105666425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839264-T-C

http://identifiers.org/hco/4/GRCh38#105666435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132839254-A-C

105666435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839254-A-G

105666442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839248-T-A

105666469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839225-T-C

105666469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839225-T-G

105666532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132839162-G-A

105666763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838962-A-G

105666763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838962-A-T

105666863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132838743-A-G

105666933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838534-T-C

105666995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838478-T-C

105667004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838467-A-G

105667004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838467-A-T

http://identifiers.org/hco/4/GRCh38#105667012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838459-C-A

105667012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838459-C-T

http://identifiers.org/hco/4/GRCh38#105667028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838443-C-A

105667028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838443-C-T

http://identifiers.org/hco/4/GRCh38#105667034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838437-C-A

105667034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838437-C-T

105667078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838393-G-A

105667078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838393-G-C

105667090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838381-G-A

105667090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838381-G-T

105667138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132838337-C-T

105667150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132838325-G-A

105667150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132838325-G-T

http://identifiers.org/hco/4/GRCh38#105667156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838319-C-A

http://identifiers.org/hco/4/GRCh38#105667201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838274-C-A

105667201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 132838274-C-T

105667388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838092-T-C

105667418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132838060-C-G

105667442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 132838043-A-G

105667442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 132838043-A-T

http://identifiers.org/hco/4/GRCh38#105667480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132838005-C-A

105667480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132838005-C-T

105667533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132837952-G-A

105667715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837781-A-G

105667763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837738-G-A

105667818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837683-G-T

105667824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837677-G-T

105667900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837593-A-G

105667923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837488-T-C

105668372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837107-A-G

105668380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132837095-T-G

105668440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132836999-G-A

105668484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132836955-A-G

105671303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132828344-C-T

http://identifiers.org/hco/4/GRCh38#105671304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132828343-C-A

105671304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132828343-C-G

105671304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132828343-C-T

105671357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132828295-G-A

105671625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132828051-G-A

105671913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132827816-T-A

105671946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132827784-A-T

http://identifiers.org/hco/4/GRCh38#105673850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132826148-A-C

105673989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132826016-A-G

105674158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132825852-G-C

105674229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132825785-G-T

http://identifiers.org/hco/4/GRCh38#105674273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132825753-C-A

105674428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132825610-G-T

105674723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132824638-G-C

105674881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132824318-G-A

105675362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132823875-C-G

105676367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132823746-C-G

105676381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132823738-G-T

105676452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132823662-C-G

105676782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132823374-T-C

105677331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132822978-T-C

105677347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132822963-T-C

105677526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132822592-T-C

http://identifiers.org/hco/4/GRCh38#105677649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132822482-C-A

105677679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132822453-T-C

105677779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132822357-G-A

105677779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132822357-G-C

105677791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132822345-C-T

105677996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132822148-C-T

http://identifiers.org/hco/4/GRCh38#105678000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132822144-C-A

http://identifiers.org/hco/4/GRCh38#105678090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132822059-C-A

105678090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132822059-C-T

105678231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132821931-T-C

105678257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132821899-A-T

http://identifiers.org/hco/4/GRCh38#105678272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132821884-C-A

105678272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821884-C-T

105678293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821868-G-A

105678293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821868-G-C

105678293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821868-G-T

105678323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821842-T-C

105678360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821806-T-C

http://identifiers.org/hco/4/GRCh38#105678543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132821652-A-C

105678543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132821652-A-G

105680338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817439-C-G

105680338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817439-C-T

105680342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817435-C-T

105680437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817358-T-G

105680603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817227-G-C

105680806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817048-A-G

105680853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132817009-T-C

105680900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132816961-A-G

105680962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non coding transcript exon variant
orthologous variants: 132816900-G-C

105681274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132816636-T-A

105681382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132816542-G-A

105681575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132816347-T-C

105681800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132816012-A-G

http://identifiers.org/hco/4/GRCh38#105681860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132815957-C-A

105681985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132815847-A-G

105682097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132815734-T-C

105682163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132815679-T-C

http://identifiers.org/hco/4/GRCh38#105682330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132815547-C-A

105682373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132815504-T-C

105682430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132815484-A-G

105682430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132815484-A-T

http://identifiers.org/hco/4/GRCh38#105682458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132815462-C-A

105682458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132815462-C-T

105682486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non coding transcript exon variant
orthologous variants: 132815434-A-G

105682486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non coding transcript exon variant
orthologous variants: 132815434-A-T

105682734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132815177-T-C

105682944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132814967-A-G

105683175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132814736-T-A

105683409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132814473-C-T

105683712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132814199-A-G

105683857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132814078-T-A

105684315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813722-T-C

http://identifiers.org/hco/4/GRCh38#105684515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132813519-A-C

105684573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813459-T-A

http://identifiers.org/hco/4/GRCh38#105684607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132813428-C-A

105684642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813399-A-G

105684666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813377-A-G

105684811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813228-G-A

105684916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813150-C-G

105685036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813038-G-A

105685069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132813006-A-G

105686548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812973-T-A

105686561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812960-G-A

105686561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812960-G-T

105686585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812939-A-G

105686586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812938-G-A

105686586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812938-G-T

105686608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812920-T-A

105686644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812886-A-T

105686657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812875-G-T

105687128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132812438-A-G

http://identifiers.org/hco/4/GRCh38#105687158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132811527-C-A

105687384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132811313-T-C

105687420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132811276-A-G

105687545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132811166-G-T

105690297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132810524-C-T

http://identifiers.org/hco/4/GRCh38#105690439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132810367-A-C

105690840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132809996-T-C

105691531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808686-G-A

105691531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808686-G-C

105691556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808670-T-C

105691556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808670-T-G

105691563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808663-A-G

105691563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808663-A-T

105691578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808651-T-A

105691578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808651-T-G

105691865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808385-T-C

105691865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808385-T-G

105691894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808354-A-T

105691936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808314-T-C

105691938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132808312-G-T

105692776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132807792-T-C

http://identifiers.org/hco/4/GRCh38#105693021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132806871-A-C

105693069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806816-C-T

105693178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806699-A-G

105693259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806606-T-C

105693347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132806518-C-T

105693377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132806488-A-G

105693377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132806488-A-T

http://identifiers.org/hco/4/GRCh38#105693460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132806405-A-C

http://identifiers.org/hco/4/GRCh38#105693497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132806371-C-A

105693497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806371-C-T

105693523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806341-G-T

http://identifiers.org/hco/4/GRCh38#105693586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132806288-C-A

105693728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132806066-T-C

105693838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132805537-C-T

105693865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132805516-T-C

105694099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132805280-T-C

105694312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132805103-C-G

105694624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804863-C-G

105694624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804863-C-T

105694728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804755-C-G

105695280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804535-T-A

105695399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804418-A-G

105695514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 132804323-A-G

http://identifiers.org/hco/4/GRCh38#105695529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132804308-C-A

105695529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132804308-C-G

105695535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132804302-T-C

105695657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132804180-T-C

105695742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804022-C-T

http://identifiers.org/hco/4/GRCh38#105695744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132804020-A-C

105695806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803967-T-A

105695806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803967-T-C

105698893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803727-T-C

105699293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803383-A-G

105699399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803288-C-T

105699450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803240-C-T

105699459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803231-T-C

105699610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803094-T-A

105699610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803094-T-C

105699745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802759-G-T

105699766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802744-T-C

http://identifiers.org/hco/4/GRCh38#105699815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132802704-A-C

http://identifiers.org/hco/4/GRCh38#105699881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132802640-C-A

105699881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802640-C-T

105699905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802616-A-G

105699911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802610-T-C

105699974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802547-G-A

http://identifiers.org/hco/4/GRCh38#105700034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132802487-A-C

105700034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802487-A-G

105700237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132802325-G-T

105700342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802116-A-G

105700349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802109-T-C

105700355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802102-G-T

105700362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802095-G-A

105700362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802095-G-C

105700362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802095-G-T

105700508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801967-G-T

105700551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801928-C-T

105700624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801854-A-T

105700952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801564-G-A

105701161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801352-G-A

105701207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801293-A-G

105701215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801285-C-T

105701223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801277-C-T

105701256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801218-T-C

105701437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801052-T-C

105702030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132800600-T-G

105702704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799816-T-C

105703283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799658-G-A

105703327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799615-G-T

105703334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799608-T-C

105703368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799571-G-A

105703460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799488-T-C

105703467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799481-C-T

105703601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799342-T-A

105707399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798865-G-T

105707539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798742-A-G

105707670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798622-G-A

105707767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798513-A-T

http://identifiers.org/hco/4/GRCh38#105707768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132798512-A-C

105707768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798512-A-G

105707768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798512-A-T

105707827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798455-T-A

105707991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25968
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132798309-C-T