68843578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 107409749-G-A

68843653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 107409829-G-A

68843734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107409910-C-G

68843734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107409910-C-T

68843761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107409937-G-A

68843761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107409937-G-T

68843778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107409954-G-T

http://identifiers.org/hco/16/GRCh38#68843850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107410021-A-C

68843850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107410021-A-G

68843856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107410027-T-A

68843856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107410027-T-C

http://identifiers.org/hco/16/GRCh38#68843918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107410087-A-C

68843918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107410087-A-G

68844027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107410177-T-C

68844095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107410227-G-A

68844384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107410633-C-T

http://identifiers.org/hco/16/GRCh38#68844580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107410816-A-C

http://identifiers.org/hco/16/GRCh38#68859811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107415212-C-A

68859811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107415212-C-T

68859872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107415272-C-T

68859984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107415384-T-C

http://identifiers.org/hco/16/GRCh38#68860008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107415408-A-C

68860121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107415521-G-A

68860121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107415521-G-T

68860191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107415591-C-G

68860191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107415591-C-T

68860468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107415868-C-G

68860535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107415935-A-G

68860544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107415944-G-T

68860583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107415978-T-C

68862511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107418835-G-A

68862566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107418888-C-T

68862756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107419053-G-A

http://identifiers.org/hco/16/GRCh38#68862889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107419147-C-A

http://identifiers.org/hco/16/GRCh38#68862931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107419185-C-A

68862931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107419185-C-T

http://identifiers.org/hco/16/GRCh38#68862974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107419228-C-A

68862979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107419233-G-C

68862979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107419233-G-T

http://identifiers.org/hco/16/GRCh38#68863057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107419311-C-A

68863057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107419311-C-G

68863136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107419381-T-A

68863136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107419381-T-G

68863142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107419387-A-T

http://identifiers.org/hco/16/GRCh38#68863165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107419410-C-A

68863180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107420127-T-C

http://identifiers.org/hco/16/GRCh38#68863230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107420177-C-A

68863230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107420177-C-T

68863276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107420220-C-G

68863293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107420233-A-G

68867042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107422044-G-T

68867109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422111-T-A

68867113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422115-G-A

68867113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422115-G-C

68867113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422115-G-T

68867123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107422131-T-C

68867134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422142-G-A

68867134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107422142-G-T

68867235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107422243-G-T

http://identifiers.org/hco/16/GRCh38#68875070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107423155-C-A

68875070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107423155-C-G

68875076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107423161-T-C

68875086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107423171-A-G

68875167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: synonymous variant
orthologous variants: 107423249-T-G

68875194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: synonymous variant
orthologous variants: 107423276-T-C

68875405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107423481-G-T

68878207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 107425677-A-G

http://identifiers.org/hco/16/GRCh38#68878337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107425787-C-A

68878337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425787-C-G

68878383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425830-T-G

68878411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425856-T-C

68878436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425882-G-A

68878450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425896-A-G

68878456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107425902-C-G

68880455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107426712-G-T

http://identifiers.org/hco/16/GRCh38#68880460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107426717-C-A

68880460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107426717-C-G

68880647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107426896-A-G

68884983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107431417-G-A

http://identifiers.org/hco/16/GRCh38#68885512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107431888-C-A

68888031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107433055-G-A

68888290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107433214-C-T

68888392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107433289-G-A

68889616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107436426-C-T

68889735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107436538-G-A

68889764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107436567-C-T

68890077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107437032-G-C

68890091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107437046-G-A

68890103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107437058-G-A

68890103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107437058-G-C

68891588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107438597-C-T

68891990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439176-G-A

http://identifiers.org/hco/16/GRCh38#68892018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107439202-A-C

68892025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439208-C-G

68892076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439263-G-A

68892170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439351-G-T

68892233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439427-A-G

68892400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107439593-A-G

68898083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107441003-C-T

68898259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107441172-A-G

68898261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107441174-G-A

68898426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107441304-C-T

68898427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107441305-G-A

http://identifiers.org/hco/16/GRCh38#68899833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107442614-A-C

http://identifiers.org/hco/16/GRCh38#68900093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107442923-C-A

68900093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107442923-C-T

http://identifiers.org/hco/16/GRCh38#68900112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107442941-C-A

http://identifiers.org/hco/16/GRCh38#68900137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107442966-C-A

68900137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107442966-C-T

68900150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107442980-A-G

http://identifiers.org/hco/16/GRCh38#68900210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107443040-C-A

68900326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107443135-A-G

68900326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107443135-A-T

http://identifiers.org/hco/16/GRCh38#68900379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107443192-C-A

68900379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107443192-C-T

68900380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107443193-G-A

68900380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107443193-G-T

68900541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107443348-C-T

68900656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107443436-T-A

68900864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107443645-A-G

http://identifiers.org/hco/16/GRCh38#68901223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107444106-A-C

68901249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107444132-G-T

68901839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107444308-C-T

68902189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107444448-G-T

http://identifiers.org/hco/16/GRCh38#68902244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107444498-C-A

http://identifiers.org/hco/16/GRCh38#68902247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107444501-C-A

68902247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107444501-C-G

68902247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107444501-C-T

68902389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107444663-G-T

68902422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107444696-G-A

68902439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107444713-T-C

68902461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107444735-G-A

68902461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107444735-G-T

68902488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107444762-A-G

68902576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107444849-A-G

68902576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107444849-A-T

68902592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107444865-A-G

68902795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445064-C-G

68902795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445064-C-T

68902828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107445099-T-C

68902851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445122-G-T

68902856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445127-T-C

68902961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445354-A-G

68903109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445626-G-A

68903162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107445673-G-T

http://identifiers.org/hco/16/GRCh38#68903287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107445796-A-C

68907361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107447199-T-C

68907361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107447199-T-G

http://identifiers.org/hco/16/GRCh38#68907416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107447259-C-A

68907423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107447266-A-G

68907444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107447287-G-A

68907444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107447287-G-T

68907470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107447310-C-T

68907545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: synonymous variant
orthologous variants: 107447385-G-A

68907573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 107447413-A-G

http://identifiers.org/hco/16/GRCh38#68907643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107447478-C-A

68907643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447478-C-T

68907644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447479-A-G

68907673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447508-G-A

68907673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447508-G-T

68907717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447552-T-C

68907812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447658-A-G

68908039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447884-T-C

http://identifiers.org/hco/16/GRCh38#68908129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107447960-C-A

68908141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107447969-G-C

68908329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107448109-G-A

68908375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107448147-T-G

http://identifiers.org/hco/16/GRCh38#68909393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107451908-C-A

68909393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 107451908-C-T

68909506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107452170-G-T

68909581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107452238-G-A

68909581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 107452238-G-T

68909626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107452288-T-C

68909672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107452336-G-T

68910259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107454051-C-T

68910505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107454272-C-G

68910617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107454386-G-A

68910652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107454421-C-T

68916030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107460047-G-A

68916856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107460807-A-G

http://identifiers.org/hco/16/GRCh38#68917241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107461253-C-A

68917318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107461322-T-C

68918869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462103-A-G

68918932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462189-C-T

http://identifiers.org/hco/16/GRCh38#68919014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107462253-A-C

68919014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462253-A-G

68919031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462266-T-C

68919046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462281-T-C

68919249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462481-T-A

68919396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462620-A-G

68919408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462628-C-T

68919493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462714-T-C

68919582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462780-C-T

68919589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107462794-T-A

68920241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107463470-G-A

68920351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107463606-G-A

68920455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107463755-G-C

68920730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107464260-G-A

68921507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107464421-T-A

68921507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107464421-T-C

http://identifiers.org/hco/16/GRCh38#68921659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107464533-C-A

68921659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 107464533-C-T

68922166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107465421-A-G

http://identifiers.org/hco/16/GRCh38#68922880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107465741-C-A

68922957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107465820-T-C

68923343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 107466147-C-T

68923344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 107466148-T-C

68923426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 107466185-G-A

68923682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107466303-T-C

68924153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107467202-T-C

68927421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 107468534-A-G

68927714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107468791-C-T

68927751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107468828-G-C

68927751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107468828-G-T

68927756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 107468833-G-A

68927863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107468910-G-A

68927931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107468951-T-C

68927938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107468958-G-A

68927938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107468958-G-T

http://identifiers.org/hco/16/GRCh38#68928049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107469069-C-A

http://identifiers.org/hco/16/GRCh38#68928136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107469138-A-C

68928191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107469165-T-C

68928341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107469208-G-T

68928354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107469221-G-T

68929436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472825-A-G

68929452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472841-G-A

68929498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472881-T-C

68929545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472917-C-T

68929570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472966-G-A

68929570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107472966-G-C

68929817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107473212-C-T

68929957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107473554-T-G

68930153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107473847-A-T

68930174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107473868-G-A

68930176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107473870-G-C

http://identifiers.org/hco/16/GRCh38#68930235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107473923-C-A

68930279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 107473967-T-G

http://identifiers.org/hco/16/GRCh38#68930347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107474011-C-A

68930347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107474011-C-T

68930366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107474017-T-A

68930366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107474017-T-C

68930374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107474025-G-A

68930374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107474025-G-T

http://identifiers.org/hco/16/GRCh38#68930391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107474042-C-A

http://identifiers.org/hco/16/GRCh38#68933772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107474965-A-C

68933879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107475078-C-T

68933920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107475119-T-C

68933924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107475123-T-C

68933988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107475185-C-T

68935660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107476410-G-A

68936636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477053-A-G

68936636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477053-A-T

68936740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477140-A-G

68936995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477736-C-T

68936997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477738-G-A

68936997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477738-G-C

68936997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477738-G-T

68937139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107477885-T-C

68937166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107477914-G-T

68937177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107477925-T-A

68937240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107477988-G-A

68948217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107481962-A-G

68948466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482173-C-G

68948583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482279-T-C

68948604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482299-C-T

68948718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482402-A-G

68949081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482713-G-A

68949104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482732-T-G

68949407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107482983-G-A

68949474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107483053-A-G

68949607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107483158-G-A

68950141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107483564-T-C

68950653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107483984-G-T

68950983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107484183-G-A

68951928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107484659-G-C

68952113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107484816-C-T

68952124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107484829-A-G

68952590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107485452-A-G

68952629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107485491-C-G

68953684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107484844-A-G

68954412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107487952-G-A

68954694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107488228-C-T

68955693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489213-G-A

68956193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489481-A-G

68956283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489565-A-G

68956348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489630-G-A

68956374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489637-T-A

68956377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107489640-A-G

68959657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107496088-C-T

68960647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107496941-T-C

68960651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107496945-C-T

68960668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107496961-T-G

68960880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107497163-T-C

68960939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107497213-G-C

68961449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107497684-C-G

68961565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107497804-A-G

68961565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107497804-A-T

68961630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107498373-C-G

68961661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107498388-G-A

68961727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107498453-A-T

68962358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107499090-T-A

68967535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107503551-T-C

http://identifiers.org/hco/16/GRCh38#68967618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107503623-C-A

68967736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107503741-T-C

68969024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504027-A-G

68969190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504144-A-G

68969190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504144-A-T

http://identifiers.org/hco/16/GRCh38#68969391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107504317-A-C

68969542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504465-C-T

68969593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504517-C-G

68969669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107504589-G-A

68970311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107505706-T-C

68972078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506112-C-T

68972096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506130-G-A

68972096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506130-G-T

68972354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506182-A-G

68972354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506182-A-T

68972641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, undefined
orthologous variants: 107506781-G-C

68972653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506793-G-A

68972684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506819-G-C

68972707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, undefined
orthologous variants: 107506842-G-A

68972807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, undefined
orthologous variants: 107506945-C-T

68972862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron variant
orthologous variants: 107506964-C-G

http://identifiers.org/hco/16/GRCh38#68972899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107507000-C-A

68972899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, undefined
orthologous variants: 107507000-C-T

68973055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107507220-G-T

68973237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107507391-T-A

68973237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107507391-T-C

68973490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107507578-G-A

68973770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107507802-G-T

68973796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107507926-G-T

http://identifiers.org/hco/16/GRCh38#68973833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107507993-A-C

68973927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107508097-G-T

68974041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107508339-G-A

68974267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107508553-T-A

http://identifiers.org/hco/16/GRCh38#68981104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107512412-A-C

68985827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107516178-C-T

68986164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107516404-A-T

http://identifiers.org/hco/16/GRCh38#68986255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107516485-C-A

68986307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107516534-C-T

68986364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107516591-A-G

http://identifiers.org/hco/16/GRCh38#68987062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107517315-A-C

http://identifiers.org/hco/16/GRCh38#68991848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107522771-A-C

68992279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107523378-A-G

68993620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107525924-T-C

68993712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107526282-A-G

68993861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107526414-C-T

68994181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107526689-T-C

68995056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107527715-A-G

68995114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107527763-A-G

68995114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107527763-A-T

68995295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107527964-C-G

68995314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107527983-A-G

68995326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107527995-G-A

68995365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107528032-C-T

68995666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107528449-T-C

68995778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107528544-G-A

http://identifiers.org/hco/16/GRCh38#68996059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107528926-C-A

68996059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107528926-C-T

http://identifiers.org/hco/16/GRCh38#68996196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107529052-C-A

69012745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530145-G-A

69012869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530289-A-G

69012869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530289-A-T

69013010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530450-C-T

69013136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530744-G-A

69013136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530744-G-T

69013184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107530794-A-G

69016437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107531953-T-C

69016469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107531985-T-C

69017176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107532808-A-G

69022781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107533634-T-A

http://identifiers.org/hco/16/GRCh38#69022967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107533812-C-A

69022967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107533812-C-T

69022991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107533836-T-C

http://identifiers.org/hco/16/GRCh38#69023079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107533900-C-A

69029086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536046-G-A

69029151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536072-A-G

69029236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536147-A-G

69029384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536293-C-T

69029454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536363-C-T

69029463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107536364-A-G

69034662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107540710-G-A

69034749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107540792-G-C

69034749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107540792-G-T

69034856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107540892-C-T

http://identifiers.org/hco/16/GRCh38#69034903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107540923-A-C

69034903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107540923-A-T

69035243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107541731-C-T

69035267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107541750-G-A

69035267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107541750-G-T

69035282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107541769-G-C

http://identifiers.org/hco/16/GRCh38#69035490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107541951-C-A

69035572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107542038-G-A

69036095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542173-G-A

69036129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542234-A-G

69036186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542292-G-A

69036196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542302-T-C

69036412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542501-C-T

69037384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542852-G-A

69037420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107542887-G-A

69037637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107543094-G-A

69037831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107543295-G-T

69038473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107543635-C-T

69038623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107543758-A-G

69039730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107544518-T-C

69039853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107544617-T-G

69039994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107544733-C-G

http://identifiers.org/hco/16/GRCh38#69040160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107544866-C-A

http://identifiers.org/hco/16/GRCh38#69040180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107544952-C-A

http://identifiers.org/hco/16/GRCh38#69040191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107544968-C-A

69040191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107544968-C-G

69040191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107544968-C-T

69040285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107545068-T-C

http://identifiers.org/hco/16/GRCh38#69040303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107545083-C-A

69040376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 107545156-T-C

69040379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 107545159-G-A

69040418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107545198-T-A

69040418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107545198-T-G

69040694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107545410-A-G

69040854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107545574-G-C

69041635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107545990-A-G

69041674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107546029-C-T

69042068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107546298-A-G

69042115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107546343-T-A

69043360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107547999-G-A

69043504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548142-G-A

69043518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548156-C-T

69043608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548241-G-T

69043647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548280-G-A

69043744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548370-A-G

69043872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548492-G-T

69043982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107548591-G-A

http://identifiers.org/hco/16/GRCh38#69044400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107549128-C-A

69048886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107556484-G-C

69048886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107556484-G-T

69049091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107556644-T-C

69049093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107556646-T-G

69049182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107556732-T-G

69055432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107558861-G-A

69055506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107558954-A-T

69055534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107558982-C-G

69056100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

69056104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

69056539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107559816-C-T

69056681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107559842-C-T

69056919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107560801-A-G

69056923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107560805-G-A

69057008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107560894-T-C

69057228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107561215-C-T

69057341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107561354-T-C

69057362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107561375-A-T

69057584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107561508-A-G

69057880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107561798-C-G

69058191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107562056-C-G

69058191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107562056-C-T

69062373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107564222-A-G

http://identifiers.org/hco/16/GRCh38#69062393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107564245-A-C

69064163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107565284-G-A

http://identifiers.org/hco/16/GRCh38#69064612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107565703-C-A

69064612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107565703-C-T

http://identifiers.org/hco/16/GRCh38#69064861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107565921-C-A

69064861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107565921-C-T

69065465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566494-T-G

69065479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566509-A-G

http://identifiers.org/hco/16/GRCh38#69065486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107566516-A-C

69065493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107566523-A-G

69065550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566576-C-T

69065583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566620-A-T

69065755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566783-C-T

69065944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107566943-T-G

69066021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107567014-C-T

69066022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107567015-G-A

69066022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107567015-G-C

69066055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107567047-G-T

69071926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107571405-C-T

69072446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572054-C-T

69072448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572056-G-A

69072448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572056-G-T

69072454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572063-G-T

69072776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572364-T-G

69072837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572423-A-G

69072938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572523-T-C

69072980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572590-G-A

69072980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107572590-G-T

69077917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575342-A-G

http://identifiers.org/hco/16/GRCh38#69078216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107575591-C-A

69078216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575591-C-T

69078222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575596-G-A

69078222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575596-G-C

69078244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575618-G-A

69078292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575661-T-C

69078405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107575772-G-A

69083455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107576780-C-T

69083742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107577071-C-G

69083743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107577072-T-C

69083790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107577123-G-A

http://identifiers.org/hco/16/GRCh38#69083808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107577143-C-A

69083808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107577143-C-T

69083854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577190-G-A

69083854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577190-G-T

69083944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577263-A-G

69084021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577307-G-T

69084257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577501-T-C

69084297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 107577508-A-G

http://identifiers.org/hco/16/GRCh38#69084444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#107577602-C-A

69084444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107577602-C-G

69084457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107577615-C-T

69084468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107577627-A-G

http://identifiers.org/hco/16/GRCh38#69084480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107577635-A-C

69084480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107577635-A-G

69084566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107577724-G-T

69084637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107577803-C-T

69084645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107577811-A-G

69084687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107578328-A-G

69084730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107578367-G-A

http://identifiers.org/hco/16/GRCh38#69084941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25749
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#107578556-C-A