http://identifiers.org/hco/11/GRCh38#112270829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50390328-C-A

112270829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50390328-C-T

112270846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390315-A-G

http://identifiers.org/hco/11/GRCh38#112270849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50390312-C-A

112270875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390286-G-A

112270875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390286-G-T

112270884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390278-A-G

112270888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390274-A-G

112270888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390274-A-T

112270902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390261-G-T

112271071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50390105-C-T

http://identifiers.org/hco/11/GRCh38#112271162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50389990-C-A

112271359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50389825-C-T

112271594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50389573-C-T

112271642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50389524-C-T

112271658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50389508-T-C

112271662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50389504-C-T

http://identifiers.org/hco/11/GRCh38#112272294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50389143-C-A

http://identifiers.org/hco/11/GRCh38#112272382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50388996-C-A

112272382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388996-C-T

112272581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388857-C-T

112272585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388853-T-C

112272635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388802-A-G

112272636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388801-T-C

112272873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50388725-A-G

112272963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50388620-A-G

112275347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50386161-T-C

112276229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50385480-G-A

112276292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50385412-G-A

112276466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50385269-T-A

http://identifiers.org/hco/11/GRCh38#112276484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50385251-A-C

112276586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50385169-A-G

112276731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50385084-T-C

http://identifiers.org/hco/11/GRCh38#112278047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50384215-C-A

112278056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50384206-G-A

112278254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50384008-G-A

112278257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50384005-T-G

112278285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50383971-C-T

112278313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50383945-T-G

112278646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50383162-C-T

112278798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50383013-C-G

112280568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50373173-T-C

112280586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50373166-G-A

http://identifiers.org/hco/11/GRCh38#112280619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50373133-C-A

112280619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50373133-C-T

112280627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50373125-G-C

112280627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50373125-G-T

http://identifiers.org/hco/11/GRCh38#112280708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50355503-C-A

http://identifiers.org/hco/11/GRCh38#112280799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50355418-C-A

112280952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50355010-A-G

112281133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50354853-G-T

112281601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50354429-T-G

112281729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50354329-G-A

112285831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353411-A-G

112285955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353309-A-T

112285977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353288-T-C

112285988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353277-C-G

112286065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353213-T-C

112286227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50353062-G-A

112286294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352995-G-A

112286349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50352935-C-T

112286483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352801-T-C

112286518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352767-C-T

112286662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352733-C-T

http://identifiers.org/hco/11/GRCh38#112286664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50352731-C-A

112287024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352356-G-A

112287104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50352279-G-A

112287406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351994-T-G

112287412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351988-C-T

112288532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351155-A-G

112288639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50351045-T-C

112288785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350887-A-G

112288785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350887-A-T

112288839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350843-C-T

112289347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350506-T-C

112289615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50350144-T-C

112289979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349732-C-T

112290137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50349610-G-T

http://identifiers.org/hco/11/GRCh38#112290157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50349591-C-A

112290157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50349591-C-T

http://identifiers.org/hco/11/GRCh38#112290177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50349571-C-A

112290177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50349571-C-T

http://identifiers.org/hco/11/GRCh38#112290226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50349518-C-A

112290227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349517-T-A

112290227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349517-T-C

112290241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349503-G-T

http://identifiers.org/hco/11/GRCh38#112290258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50349488-C-A

112290298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349449-G-A

112290325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349425-G-A

112290334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349416-G-A

112290334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349416-G-T

112290385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349364-C-T

112290512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50349251-G-T

112290872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348894-G-A

112291169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50348628-T-G

112291297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50348541-G-A

112291345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50348509-G-A

http://identifiers.org/hco/11/GRCh38#112291446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50348419-C-A

112291459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50348406-A-G

112291489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50348375-C-T

112291537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347792-A-G

112291668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347693-G-A

112291697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347664-G-A

http://identifiers.org/hco/11/GRCh38#112291814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50347295-C-A

112291814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347295-C-T

112291912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347202-G-T

112291930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347185-T-A

112291994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347125-A-G

112291995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347124-C-T

112292012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347100-T-A

112292033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50347051-T-C

112292105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346964-G-T

http://identifiers.org/hco/11/GRCh38#112292146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50346930-C-A

112292178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346898-A-T

112292364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346708-T-C

112292374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346689-G-T

112292489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346430-T-C

112292539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346374-A-G

112292549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50346364-A-T

http://identifiers.org/hco/11/GRCh38#112292593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50346322-A-C

http://identifiers.org/hco/11/GRCh38#112292756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50345991-C-A

112292756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345991-C-T

112292815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50345936-T-C

112292825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345926-C-G

http://identifiers.org/hco/11/GRCh38#112292918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#50345826-C-A

112292933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345788-A-G

112293017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50345682-A-G

112293079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50345620-A-G

112293170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345529-A-G

112293170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345529-A-T

112293173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50345526-T-C

112293428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 50345302-T-A

112297171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343604-G-A

112297433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343367-C-T

112297434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343366-G-A

112297469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50343331-T-C

112297896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342782-C-T

112297943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342747-G-C

112297969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342721-C-T

112297979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342711-G-A

112297979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342711-G-C

112297979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342711-G-T

112298823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50342448-G-A

http://identifiers.org/hco/11/GRCh38#112298905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50342368-C-A

112299238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341919-G-A

112299238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341919-G-T

112299878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341400-T-G

http://identifiers.org/hco/11/GRCh38#112299962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50341370-A-C

112300104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341247-G-A

112300136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341217-T-A

112300136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341217-T-C

112300231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50341124-C-T

112300554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340819-G-A

112300554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340819-G-C

http://identifiers.org/hco/11/GRCh38#112300668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50340708-C-A

112300668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340708-C-T

112300750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340656-A-G

112300809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50340601-T-C

112302161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339921-T-A

112302161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339921-T-G

112302287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339797-T-C

112302438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339645-C-T

112302446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339637-G-A

112303152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50339117-G-A

112303748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50338551-G-A

112305285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50337674-T-G

112306111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336965-G-C

112306122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336954-A-T

112306246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336850-C-T

112306256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336840-G-A

http://identifiers.org/hco/11/GRCh38#112306498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50336587-C-A

112306998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50336080-G-A

112307114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335968-C-G

112307146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335942-G-A

112307146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335942-G-C

112307201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335889-A-G

112309093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335207-C-T

112309181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50335119-C-T

http://identifiers.org/hco/11/GRCh38#112309352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50334953-A-C

112309818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50334456-A-T

112310139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333957-C-T

112310491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333622-C-T

112310620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333525-G-A

http://identifiers.org/hco/11/GRCh38#112310638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50333506-C-A

112310638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333506-C-G

112310718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50333426-A-G

112310806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333338-C-T

112311093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50333051-G-A

112311175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50332945-C-G

112311348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50332787-C-T

112311819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50332211-A-G

112312102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50331943-A-T

112312112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50331933-G-A

112312253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50331444-A-G

112312583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50331115-T-G

112312793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50328758-T-G

112312860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50328712-T-G

112312880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50328692-C-T

112313925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50325632-C-G

112313925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50325632-C-T

112315365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324707-C-G

112315504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324572-T-A

112315689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324389-G-T

112315771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324331-C-T

112315828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324264-C-T

112315946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50324176-A-G

112316149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50323994-C-T

112316209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50323935-T-C

112319759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321557-G-C

112319870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321443-A-G

112319881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321432-C-T

112319899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321414-C-T

112319942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321377-G-A

http://identifiers.org/hco/11/GRCh38#112320074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50321244-A-C

112320074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321244-A-T

112320094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50321228-G-A

http://identifiers.org/hco/11/GRCh38#112321447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50320485-C-A

112321896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50320038-G-A

112321967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319968-G-A

112321986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319949-G-A

112322109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319822-A-G

112322178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319757-A-G

112322184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319751-T-C

112322184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 50319751-T-G

112322301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319637-C-G

112322301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319637-C-T

112322335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319604-A-G

112322664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50319336-G-C

112333149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316422-A-G

112333317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316309-G-T

112333337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316289-G-A

112333371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50316255-G-A

112333589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315724-C-T

112333595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315718-C-T

112333712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315408-C-T

112334044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50315057-A-G

112334224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314415-G-A

112334305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314348-C-T

112334470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314183-C-T

112334566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314074-G-A

112334568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314072-C-T

112334627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50314017-A-T

http://identifiers.org/hco/11/GRCh38#112334820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50313851-C-A

112334938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313769-G-T

112334988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313722-G-T

112335008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50313702-G-A

112338786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50311368-G-A

112338862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50311292-C-T

112338966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50311186-A-G

http://identifiers.org/hco/11/GRCh38#112339276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#50310921-C-A

112339379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310832-C-T

112339396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310815-A-G

112339396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310815-A-T

112339594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310634-C-T

112339663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310568-T-G

112339709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310523-G-A

112339995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310241-A-G

112340104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50310113-C-T

112340772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309765-G-C

112340804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309733-G-A

112340918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309636-G-C

112340960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309596-G-A

112341075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309485-C-T

112341101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 50309460-A-G

112343383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50307662-A-G

112343386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50307659-G-A

112343450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50307604-T-A

112343503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27443
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 50307551-A-G