89608976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79335698-A-G

89609029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335752-G-A

89609029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335752-G-T

http://identifiers.org/hco/15/GRCh38#89609049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79335771-C-A

89609049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79335771-C-T

http://identifiers.org/hco/15/GRCh38#89616318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79337890-A-C

89616318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79337890-A-G

89616326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79337898-A-G

89616527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338095-A-T

89616549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338148-G-A

89616549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338148-G-T

http://identifiers.org/hco/15/GRCh38#89616565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79338164-C-A

89616565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338164-C-G

89616627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338251-T-C

89616628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338252-C-T

89617030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79338718-G-A

89617312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79338906-G-C

89617703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79339219-T-C

http://identifiers.org/hco/15/GRCh38#89618265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79339757-C-A

89618265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79339757-C-T

89618482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79339961-A-G

89619648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79340560-A-G

89619648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79340560-A-T

89621384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79341562-G-A

89621384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79341562-G-C

http://identifiers.org/hco/15/GRCh38#89621394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79341571-C-A

89621394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 79341571-C-T

89621674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342019-G-A

89621677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342022-G-A

89621677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342022-G-T

89621726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342071-C-T

89621820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342154-A-G

http://identifiers.org/hco/15/GRCh38#89622067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79342262-A-C

89622330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342337-A-G

89622469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342406-C-T

89622650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342559-C-T

89622694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342617-C-T

89622701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342624-C-T

89622855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342852-G-A

89622872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342872-A-G

89622946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79342994-G-A

89623178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343219-C-T

89623492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343309-T-G

http://identifiers.org/hco/15/GRCh38#89623512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79343328-C-A

89623578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-A

89623578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-C

89623578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343407-T-G

89623579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-A

89623579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-C

89623579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79343408-G-T

89623704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343530-T-C

89624090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343916-G-A

89624090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79343916-G-T

89624251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344062-C-G

89624251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344062-C-T

89624426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79344231-C-T

89624572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344377-G-A

89624572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344377-G-C

89624798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79344588-T-C

89624835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344628-T-C

89624970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344751-G-A

89624970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344751-G-C

89625100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79344878-G-C

http://identifiers.org/hco/15/GRCh38#89625266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345044-C-A

89625266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79345044-C-T

89625275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79345053-T-C

89625603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345387-T-C

89625603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345387-T-G

89625744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345528-T-C

http://identifiers.org/hco/15/GRCh38#89625844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345611-C-A

http://identifiers.org/hco/15/GRCh38#89625911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345658-C-A

89625911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345658-C-T

89625917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345664-C-T

89625998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79345745-C-G

89626077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345827-G-A

http://identifiers.org/hco/15/GRCh38#89626162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345872-C-A

89626162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345872-C-G

89626162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345872-C-T

http://identifiers.org/hco/15/GRCh38#89626197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79345906-C-A

89626198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345907-A-G

89626226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345933-A-G

89626282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345983-G-A

89626306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79345996-C-T

89626369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346033-A-T

89626480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346112-G-A

89626665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79346254-C-G

89626981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346427-C-T

89626987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346433-A-G

89627072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 79346566-C-T

89627286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347011-G-C

89627286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347011-G-T

89627309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347026-G-C

89627385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347070-C-G

89627488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347177-G-A

http://identifiers.org/hco/15/GRCh38#89627985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79347726-A-C

89627985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79347726-A-G

http://identifiers.org/hco/15/GRCh38#89628084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79347966-C-A

89628084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79347966-C-G

89628084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79347966-C-T

89628090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79347972-G-A

89628090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79347972-G-C

89628090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79347972-G-T

89628180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79348047-C-T

http://identifiers.org/hco/15/GRCh38#89628193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79348060-C-A

89628269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79348154-G-A

89628269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79348154-G-T

89628308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79348193-G-T

89628713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79348587-G-A

89628713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79348587-G-C

89628713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79348587-G-T

89628814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79348685-C-T

89628833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79348708-C-T

89628953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79348886-T-C

89628978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79348900-C-G

89628992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79348914-A-G

89629210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349110-T-A

89629210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349110-T-G

89629211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349111-G-A

89629211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349111-G-T

89629218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349118-G-A

89629218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349118-G-T

89629378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 79349138-G-A

89629378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79349138-G-C

89629378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79349138-G-T

89629400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79349160-C-T

89629495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79349255-T-G

89629508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79349268-C-T

89629522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79349282-G-T

http://identifiers.org/hco/15/GRCh38#89629526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349286-C-A

89629526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79349286-C-G

89629526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79349286-C-T

89629640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349397-A-G

http://identifiers.org/hco/15/GRCh38#89629711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349448-A-C

89629711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349448-A-G

89629711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349448-A-T

89629765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349484-G-A

89629765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349484-G-T

89629766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349485-G-A

89629766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349485-G-C

89629766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349485-G-T

89629963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349672-A-G

http://identifiers.org/hco/15/GRCh38#89630085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349774-A-C

89630085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349774-A-G

http://identifiers.org/hco/15/GRCh38#89630181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79349845-C-A

89630181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349845-C-T

89630186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349850-G-C

89630186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79349850-G-T

89630491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 79350134-C-T

89630512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350155-G-A

89630512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350155-G-C

89630512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350155-G-T

89630560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350205-T-C

89630560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350205-T-G

89630575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350220-G-A

89630575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350220-G-T

http://identifiers.org/hco/15/GRCh38#89630595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350240-A-C

http://identifiers.org/hco/15/GRCh38#89630641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350280-C-A

89630641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350280-C-G

89630641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79350280-C-T

http://identifiers.org/hco/15/GRCh38#89631351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350563-C-A

89631351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350563-C-G

89631351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350563-C-T

89631409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350597-G-A

89631409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350597-G-T

89631436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350625-G-A

89631436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350625-G-C

89631436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350625-G-T

89631442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350631-A-G

89631442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79350631-A-T

89631488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79350689-A-G

89631488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79350689-A-T

http://identifiers.org/hco/15/GRCh38#89631570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79350772-C-A

89631570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79350772-C-G

89632258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351408-C-T

89632269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351420-C-T

89632361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351509-T-C

89632409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351586-C-T

89632525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351689-T-C

89632655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351811-G-T

89632716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79351825-T-C

89632847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79351881-C-T

89632904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79351938-G-A

89632904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79351938-G-T

89632907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79351941-G-A

89632907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79351941-G-C

http://identifiers.org/hco/15/GRCh38#89632919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79351953-C-A

89632919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79351953-C-T

89633079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79352105-A-G

89633249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79352309-A-G

89633249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79352309-A-T

http://identifiers.org/hco/15/GRCh38#89633568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79352453-C-A

89633622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352505-G-A

89633622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352505-G-T

89633692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79352533-G-A

89633692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79352533-G-T

89633820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: stop gained
orthologous variants: 79352661-G-A

89633820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79352661-G-C

89633820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79352661-G-T

http://identifiers.org/hco/15/GRCh38#89633836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79352677-C-A

89633836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79352677-C-T

89633906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352747-T-C

89633906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352747-T-G

89633943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352784-G-A

89633943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352784-G-T

http://identifiers.org/hco/15/GRCh38#89633954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79352795-A-C

89633954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352795-A-G

89633996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352864-T-A

89633996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352864-T-C

89633996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79352864-T-G

89641868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354103-G-A

89641923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354163-G-A

89641928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354168-G-A

89641938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354178-G-A

http://identifiers.org/hco/15/GRCh38#89642059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79354266-C-A

89642059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354266-C-T

http://identifiers.org/hco/15/GRCh38#89642067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79354273-C-A

89642067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354273-C-T

89642070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354276-T-C

89642073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354279-A-G

89642075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354281-G-A

89642075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354281-G-T

http://identifiers.org/hco/15/GRCh38#89642099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79354312-C-A

89642099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354312-C-T

89642105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354318-G-A

89642105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354318-G-T

89642112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354325-G-C

89642112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354325-G-T

89642227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354399-G-A

89642227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354399-G-C

89642227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354399-G-T

89642290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354462-G-A

89642290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354462-G-C

89642290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79354462-G-T

http://identifiers.org/hco/15/GRCh38#89642381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79354553-C-A

89642381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79354553-C-T

89642455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354627-G-C

89642455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354627-G-T

89642504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354685-G-T

http://identifiers.org/hco/15/GRCh38#89642514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79354695-C-A

89642526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354705-A-T

89642848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79354843-C-T

89643051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79355029-C-T

89644789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356301-T-C

89644871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356340-A-G

89644898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356368-G-T

http://identifiers.org/hco/15/GRCh38#89644903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79356373-C-A

89644903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356373-C-T

89644925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356395-T-A

89644925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356395-T-C

89644933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356402-G-A

89644933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356402-G-T

89644980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356452-G-A

89644980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356452-G-T

89645201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356672-C-G

89645414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79356815-G-A

89645554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356956-T-C

89645565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356967-A-G

89645565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79356967-A-T

http://identifiers.org/hco/15/GRCh38#89645756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79357136-C-A

89645765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357145-A-G

89645765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357145-A-T

89645824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357204-A-G

89645824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357204-A-T

89645972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79357371-G-A

89645972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79357371-G-C

89645972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79357371-G-T

89646050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357460-T-G

89646092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357506-C-G

89646092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357506-C-T

89646105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357517-T-C

http://identifiers.org/hco/15/GRCh38#89646107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79357519-C-A

89646107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357519-C-T

http://identifiers.org/hco/15/GRCh38#89646131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79357543-C-A

89646131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357543-C-G

89646131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357543-C-T

89646158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357566-G-A

89646158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357566-G-T

89646161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357569-G-T

89646168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357582-G-A

89646168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357582-G-T

89646308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357684-C-T

89646367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357743-G-A

89646526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357920-T-A

89646545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357939-T-G

89646571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357948-C-T

89646579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79357956-G-C

89646716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358093-G-C

89646716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358093-G-T

89646877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79358208-G-C

89646877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79358208-G-T

http://identifiers.org/hco/15/GRCh38#89646910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79358241-C-A

89646910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79358241-C-G

89647022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79358353-C-G

http://identifiers.org/hco/15/GRCh38#89647072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79358403-C-A

89647072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358403-C-T

89647158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358505-G-A

89647158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358505-G-T

89647165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358512-A-G

89647204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358558-T-A

89647304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358658-A-G

89647466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358816-A-T

http://identifiers.org/hco/15/GRCh38#89647520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79358856-C-A

89647520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79358856-C-T

http://identifiers.org/hco/15/GRCh38#89647524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79358860-A-C

http://identifiers.org/hco/15/GRCh38#89647575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79358893-A-C

89647641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79358959-G-A

89647641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79358959-G-C

89647641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79358959-G-T

http://identifiers.org/hco/15/GRCh38#89647700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79359018-C-A

89647700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79359018-C-T

89647792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79359125-G-A

89647792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79359125-G-T

89648109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79359698-G-A

89648109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79359698-G-T

89648194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79359757-T-C

89648264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359802-G-A

http://identifiers.org/hco/15/GRCh38#89648420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79359958-C-A

89648420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359958-C-G

89648420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359958-C-T

http://identifiers.org/hco/15/GRCh38#89648423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79359961-C-A

89648423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79359961-C-G

89648423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359961-C-T

89648450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359988-G-A

89648450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79359988-G-T

89648486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79360024-G-A

89648486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: synonymous variant
orthologous variants: 79360024-G-T

http://identifiers.org/hco/15/GRCh38#89648489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79360027-C-A

89648489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79360027-C-G

89648489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79360027-C-T

89648490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79360028-A-G

89648490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: missense variant
orthologous variants: 79360028-A-T

http://identifiers.org/hco/15/GRCh38#89648625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79360163-C-A

89648625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360163-C-T

89648683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360221-T-A

89648683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360221-T-G

http://identifiers.org/hco/15/GRCh38#89648714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79360252-A-C

89648791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360329-G-T

http://identifiers.org/hco/15/GRCh38#89648902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79360395-C-A

89648902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360395-C-T

89648915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360408-G-A

89648915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360408-G-T

89648988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360465-G-A

89648988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360465-G-T

89649033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360510-G-T

89649095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360572-G-A

89649095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360572-G-C

89649095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360572-G-T

89649186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360663-G-A

89649270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360747-G-T

89649311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360788-G-A

89649311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360788-G-C

89649311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79360788-G-T

89649357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79360834-C-T

89649373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79360850-G-A

89649373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 79360850-G-C

http://identifiers.org/hco/15/GRCh38#89649384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79360859-C-A

89649384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360859-C-G

89649384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360859-C-T

89649528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79360936-C-T

89649597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361004-G-A

http://identifiers.org/hco/15/GRCh38#89649639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361043-C-A

http://identifiers.org/hco/15/GRCh38#89649658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361062-C-A

89649658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361062-C-T

http://identifiers.org/hco/15/GRCh38#89649659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361063-C-A

89649659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361063-C-T

http://identifiers.org/hco/15/GRCh38#89649662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361066-A-C

89650009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79361433-G-T

http://identifiers.org/hco/15/GRCh38#89650010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361434-C-A

89650011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 79361435-T-C

http://identifiers.org/hco/15/GRCh38#89650083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79361504-C-A

89650083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361504-C-T

89650117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361534-T-C

89650146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79361554-G-A

89651976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363127-C-G

http://identifiers.org/hco/15/GRCh38#89652203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79363278-A-C

89652203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363278-A-G

http://identifiers.org/hco/15/GRCh38#89652478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79363490-A-C

89652478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363490-A-G

89652481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363492-G-A

89652481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363492-G-C

http://identifiers.org/hco/15/GRCh38#89652488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79363499-C-A

89652488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363499-C-G

89652488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363499-C-T

89652523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363535-A-G

89652523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363535-A-T

89652524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363536-G-A

89652524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363536-G-C

89652524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79363536-G-T

89652824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79363800-C-T

http://identifiers.org/hco/15/GRCh38#89652841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79363817-C-A

89652886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 79363862-T-C

89652899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79363875-G-A

89652899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79363875-G-T

89652906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79363882-G-A

89652906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79363882-G-T

89653119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79364054-T-C

89653236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79364206-C-T

89654951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365136-C-G

89655212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79365299-G-A

89655240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79365328-G-C

89655294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365358-C-T

89655318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365377-A-G

89655351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365388-C-T

89655361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365398-G-C

89655361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365398-G-T

89655411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365425-A-G

89655411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365425-A-T

http://identifiers.org/hco/15/GRCh38#89655414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365428-C-A

89655414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 79365428-C-T

89655436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79365450-A-G

89655436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79365450-A-T

http://identifiers.org/hco/15/GRCh38#89655446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365460-C-A

89655446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79365460-C-G

89655446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 79365460-C-T

89655453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79365467-G-T

http://identifiers.org/hco/15/GRCh38#89655510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365524-A-C

http://identifiers.org/hco/15/GRCh38#89655517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365531-A-C

89655517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79365531-A-G

89655517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79365531-A-T

89655575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79365586-G-A

89655575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79365586-G-C

89655575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79365586-G-T

http://identifiers.org/hco/15/GRCh38#89655590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365601-C-A

89655590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79365601-C-T

89655591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron_variant, undefined
orthologous variants: 79365602-G-A

http://identifiers.org/hco/15/GRCh38#89655680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365700-C-A

http://identifiers.org/hco/15/GRCh38#89655902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#79365892-A-C

89656701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79367172-A-G

89656740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79367236-A-G

89657495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30497
most severe consequence: intron variant
orthologous variants: 79367664-G-T