78943531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352281-C-G

78943551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352301-A-G

http://identifiers.org/hco/10/GRCh38#78943575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25352324-C-A

78943589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352338-T-C

78943589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352338-T-G

http://identifiers.org/hco/10/GRCh38#78943607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25352355-C-A

78943607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352355-C-T

78943643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352389-G-T

http://identifiers.org/hco/10/GRCh38#78943655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25352401-C-A

78943655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352401-C-G

78943665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25352441-G-T

http://identifiers.org/hco/10/GRCh38#78943708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25352486-C-A

78944697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25354016-C-G

78944697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25354016-C-T

78944699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25354018-G-A

http://identifiers.org/hco/10/GRCh38#78944746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25354068-C-A

78944746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 25354068-C-T

78944766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354088-A-G

78944786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25354108-G-C

78944786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25354108-G-T

78944843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354166-A-G

http://identifiers.org/hco/10/GRCh38#78944845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25354168-A-C

78944845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354168-A-G

78944851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25354174-T-C

http://identifiers.org/hco/10/GRCh38#78944867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25354190-C-A

78944901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354233-C-T

78944934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354266-G-A

78944934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354266-G-C

78945041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354384-C-T

http://identifiers.org/hco/10/GRCh38#78945225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25354555-C-A

78945225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354555-C-T

78945229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354559-G-A

78945246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25354574-C-T

78945501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25354782-C-T

78945794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355071-T-C

78945904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25355171-T-C

http://identifiers.org/hco/10/GRCh38#78946003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25355262-C-A

78946003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355262-C-T

http://identifiers.org/hco/10/GRCh38#78946045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25355304-C-A

78946062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355320-A-G

http://identifiers.org/hco/10/GRCh38#78946069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25355338-C-A

78946381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355667-G-A

78946381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355667-G-T

78946440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355726-G-C

78946536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355826-G-A

78946666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25355966-A-G

78946703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356003-C-T

78946745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356044-G-A

78947705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356726-C-G

http://identifiers.org/hco/10/GRCh38#78947706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25356727-C-A

78947794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356807-T-C

78947828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356820-A-G

78947846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356839-G-C

78947925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25356916-A-G

78949354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357360-A-G

78950008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357962-C-G

78950019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357973-G-A

http://identifiers.org/hco/10/GRCh38#78950036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25357990-C-A

78950036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25357990-C-T

http://identifiers.org/hco/10/GRCh38#78950120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25358074-C-A

78950120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358074-C-T

78950799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358161-C-G

78950799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358161-C-T

78950922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358289-C-G

78950922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358289-C-T

http://identifiers.org/hco/10/GRCh38#78950940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25358307-A-C

http://identifiers.org/hco/10/GRCh38#78951191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25358541-C-A

http://identifiers.org/hco/10/GRCh38#78951551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25358945-C-A

78951551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25358945-C-T

78951841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359224-C-T

78951860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359243-A-T

http://identifiers.org/hco/10/GRCh38#78951957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25359348-A-C

78951984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359379-T-C

78952074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359467-C-G

78952115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359509-G-T

78952188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359582-T-C

78952384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25359904-A-G

78952616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25360136-G-A

78953475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25360957-G-A

78953494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25360975-C-T

78953528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25361087-G-A

78953717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25361277-G-C

78953793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25361351-C-G

78955429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362344-G-A

78955522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362435-G-C

78956100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362490-G-A

78956184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362578-C-T

78956265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362656-G-A

http://identifiers.org/hco/10/GRCh38#78956439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25362830-C-A

78956544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362886-C-G

78956545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25362887-G-A

78956748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363097-C-G

78956820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363179-G-C

78957378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363701-T-C

78957442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363746-C-G

78957500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25363803-A-T

78957727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364088-G-T

http://identifiers.org/hco/10/GRCh38#78957759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25364120-A-C

78957759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364120-A-G

78957776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364137-T-A

78957776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364137-T-C

78957812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364173-T-C

78957899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364281-T-C

78957922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364304-A-G

78957975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364424-A-T

http://identifiers.org/hco/10/GRCh38#78958095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25364542-C-A

78958167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25364618-C-T

http://identifiers.org/hco/10/GRCh38#78959220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25365340-C-A

78959610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25365615-G-T

78959749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25365784-G-A

78959749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25365784-G-T

78959941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25365976-C-T

78960109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366089-T-C

78960287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366236-G-T

78960326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366275-T-C

78960369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366318-G-T

78960627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25366555-G-A

78960636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25366563-G-A

78960636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25366563-G-T

78960733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366658-C-T

78960750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25366675-G-T

http://identifiers.org/hco/10/GRCh38#78960824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25366753-C-A

78960896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366806-T-C

78961104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25366949-T-C

78961189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367030-T-C

78961211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367052-G-A

78961211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25367052-G-T

http://identifiers.org/hco/10/GRCh38#78961338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25367172-C-A

78961427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25367852-G-T

78961471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25367896-T-C

78961475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25367900-A-G

78961560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25367973-G-C

78961621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25368020-A-G

78963849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25370896-C-T

78963893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25370937-C-T

78964275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25371291-G-A

78964461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25371499-T-C

78964488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25371524-C-T

78964592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25371621-C-T

http://identifiers.org/hco/10/GRCh38#78965115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25372091-C-A

78965115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25372091-C-T

78965116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25372092-G-A

78965116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25372092-G-C

78965443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25372414-G-A

78965829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25372777-A-T

78965959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25372907-C-T

78966020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25372980-T-A

78966042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373002-C-T

78966187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373126-G-A

78966423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373329-G-A

78966561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373464-A-G

78966653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373547-G-A

http://identifiers.org/hco/10/GRCh38#78966792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25373620-A-C

78966907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25373726-C-T

78967691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25374443-G-A

78969688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25374894-G-A

78969731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25374928-T-C

http://identifiers.org/hco/10/GRCh38#78969789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25375009-C-A

78969789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375009-C-T

78969808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375026-G-A

78969931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375142-C-T

78969950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375171-G-A

78970036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25375282-G-A

http://identifiers.org/hco/10/GRCh38#78970174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25375433-C-A

http://identifiers.org/hco/10/GRCh38#78970921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25375984-C-A

78971010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376054-C-T

78971035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376079-T-C

78971750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376692-G-A

http://identifiers.org/hco/10/GRCh38#78971927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25376840-A-C

78972008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376916-G-A

78972086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25376962-C-T

78972185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377043-G-A

78972234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377092-C-T

78972290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377142-C-T

78972416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377256-C-G

78972454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377293-T-G

78972469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377310-T-C

78972496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377334-G-A

78972496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377334-G-T

78972551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377388-C-T

78972633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377473-G-C

78972656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377488-C-T

78972667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377499-G-A

78972828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377651-C-T

78972829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377652-G-A

78972853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377723-G-A

78972871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377741-T-C

78972941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377819-G-T

78973108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377954-T-C

78973124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25377968-C-G

http://identifiers.org/hco/10/GRCh38#78973171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25378009-C-A

78973171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378009-C-G

78973171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378009-C-T

78973419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378300-A-G

78973442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378317-C-G

78973906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378733-C-G

78973993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25378756-G-C

http://identifiers.org/hco/10/GRCh38#78974017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25378780-A-C

http://identifiers.org/hco/10/GRCh38#78974221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25378988-C-A

78974285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379064-G-C

78974361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379145-G-A

78974479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379259-T-C

78974518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379292-A-T

78974940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25379704-C-T

78975206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25379867-T-G

78976102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380535-G-A

78976312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380655-C-T

78976683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380846-C-T

78976778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25380949-T-C

78976851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381017-C-T

http://identifiers.org/hco/10/GRCh38#78976945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25381102-C-A

78976995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381144-G-T

78977084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381209-A-G

http://identifiers.org/hco/10/GRCh38#78977167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25381276-C-A

78977167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381276-C-T

78977172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381282-T-C

78977181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25381291-C-G

78978345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382198-A-G

http://identifiers.org/hco/10/GRCh38#78978502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25382363-A-C

78978845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382405-G-T

78978852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382412-G-A

78978919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382472-T-A

78979933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25382875-C-T

78980197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383386-G-A

78980209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383392-G-A

78980320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383500-A-T

78980696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383904-T-C

78980700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383908-A-G

78980744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25383954-C-G

78980826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384037-C-G

78980826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384037-C-T

78980925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384149-C-G

78981057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384255-G-A

78981260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384437-C-T

78981261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384438-C-T

78981425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384550-T-C

78981567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384664-C-G

http://identifiers.org/hco/10/GRCh38#78981785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25384890-C-A

78981862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25384977-G-A

78981948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385057-T-A

78982046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25385149-C-T

78982059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25385164-G-C

78982127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25385212-G-A

78982140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385222-G-A

78982140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385222-G-C

78982187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25385253-C-T

78982349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25385378-C-T

78982643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385648-C-T

78982699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385680-G-T

78982762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385705-C-T

78983006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385929-G-A

78983006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385929-G-C

78983061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25385968-C-T

http://identifiers.org/hco/10/GRCh38#78983224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25386119-A-C

78983225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386120-G-A

78983289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386182-C-T

78983295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386188-G-T

78983316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386208-C-G

78983662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386454-T-C

78983702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386494-C-T

78983732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386525-C-T

78983957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386709-G-A

78984018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386769-T-C

78984206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25386943-T-C

78984294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387024-T-A

78984315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387033-T-C

78984593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387217-A-T

78984620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387244-G-T

78984693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387320-T-A

78985033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387673-G-A

78985081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387725-A-G

78985081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25387725-A-T

http://identifiers.org/hco/10/GRCh38#78985674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25388354-C-A

78985674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388354-C-G

78985674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388354-C-T

http://identifiers.org/hco/10/GRCh38#78985728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25388412-C-A

78985728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388412-C-T

78985759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388441-A-G

78986377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388924-G-A

78986399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25388946-C-G

78986578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389006-G-T

78986663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389061-G-T

78987126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25389605-G-A

http://identifiers.org/hco/10/GRCh38#78993620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25395316-A-C

78993621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395317-G-A

78993682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395375-T-C

78993683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395376-G-T

78993790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395474-G-C

78994006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395681-C-T

78994081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395756-A-G

78994264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25395933-G-A

78994418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396659-G-C

78994591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396826-C-G

78994591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25396826-C-T

78995579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25397259-A-G

78995608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25397289-G-A

78995610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25397291-G-A

http://identifiers.org/hco/10/GRCh38#78996728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25398343-C-A

http://identifiers.org/hco/10/GRCh38#78997007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25398547-A-C

78997007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398547-A-T

http://identifiers.org/hco/10/GRCh38#78997018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25398558-A-C

78997062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398614-C-T

78997346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25398868-T-G

78997737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399083-C-T

78997767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399110-T-C

78998146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399496-G-A

78998221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25399551-T-G

78999041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399909-C-T

78999170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399983-C-G

78999187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25399999-G-A

78999268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400086-T-C

78999276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400094-G-T

78999478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400298-T-C

78999659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400539-T-C

78999992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400839-A-G

http://identifiers.org/hco/10/GRCh38#79000003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25400850-C-A

79000074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25400959-T-C

79000150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401078-T-C

79000352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401277-G-T

79000418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25401333-T-C

http://identifiers.org/hco/10/GRCh38#79000469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25401376-C-A

79000608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401608-G-T

http://identifiers.org/hco/10/GRCh38#79000659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25401626-C-A

79000660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401627-T-C

http://identifiers.org/hco/10/GRCh38#79000718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25401682-C-A

79000719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401683-G-A

79000719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401683-G-T

79000723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401687-A-G

79000759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401722-G-T

79000793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401787-T-C

79000818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401812-C-G

79000818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401812-C-T

http://identifiers.org/hco/10/GRCh38#79000829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25401819-C-A

79000829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401819-C-T

http://identifiers.org/hco/10/GRCh38#79000835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25401825-C-A

79000835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401825-C-T

79000863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401856-T-C

79000906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25401905-T-C

79001040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402032-G-A

79001046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402038-T-C

79001111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402097-G-T

http://identifiers.org/hco/10/GRCh38#79001150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25402134-C-A

79001150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402134-C-T

http://identifiers.org/hco/10/GRCh38#79001167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25402151-C-A

79001167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402151-C-T

79001174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402158-T-C

79001190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402174-G-A

79001222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402208-T-C

79001259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25402243-T-A

79001259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25402243-T-C

http://identifiers.org/hco/10/GRCh38#79001471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25402450-C-A

79001522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402497-G-A

79001522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402497-G-T

79001592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402536-G-A

79001592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402536-G-T

79001599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402543-G-T

http://identifiers.org/hco/10/GRCh38#79001653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25402595-C-A

79001653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402595-C-T

79001668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25402610-A-G

79001700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402642-G-T

79001701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402643-G-T

79001735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402671-G-A

79001735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402671-G-T

79001745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402681-A-G

79001797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402722-G-A

http://identifiers.org/hco/10/GRCh38#79001831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25402760-C-A

79001831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402760-C-T

79001876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402771-T-C

79002032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402885-T-C

79002041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402894-G-A

79002041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402894-G-T

79002070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402923-A-G

79002118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402942-T-A

79002118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402942-T-C

79002122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402946-T-A

79002122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402946-T-C

79002123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402947-G-A

79002123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402947-G-C

79002123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402947-G-T

79002178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25402988-A-G

79002222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25403044-T-A

79002222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25403044-T-C

79002222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25403044-T-G

http://identifiers.org/hco/10/GRCh38#79002749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25403442-A-C

79002852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403539-G-A

http://identifiers.org/hco/10/GRCh38#79002934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25403601-C-A

79002955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403622-G-T

79003232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403749-A-T

http://identifiers.org/hco/10/GRCh38#79003441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25403794-C-A

79003490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403836-G-A

79003490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25403836-G-C

79003747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25404007-A-G

79003754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25404014-T-G

79003772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25404032-G-T

79003790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25404049-G-A

79003809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404067-A-G

79003817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404075-G-A

79003880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25404136-G-A

http://identifiers.org/hco/10/GRCh38#79003926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25404183-C-A

79004002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404245-A-G

79004258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404474-G-A

79004272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404489-G-A

79004348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404552-G-A

79004447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404652-T-G

http://identifiers.org/hco/10/GRCh38#79004476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25404686-C-A

79004584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404795-C-T

79004595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25404806-T-A

79005087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405308-G-C

79005177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25405486-G-A

79005756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406116-C-T

79005775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406140-C-T

79005780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25406141-G-A

79008659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407534-G-C

79008805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407667-T-G

79009171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25407899-C-T

79010212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25408823-G-C

79010405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409000-T-C

http://identifiers.org/hco/10/GRCh38#79010423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25409019-C-A

79010619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409488-G-T

http://identifiers.org/hco/10/GRCh38#79010807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25409631-C-A

79010959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409800-C-G

79010959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409800-C-T

79011025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25409852-T-G

79012866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25410330-G-A

79012866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25410330-G-C

79012944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410395-C-T

79013140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410521-C-G

79013140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410521-C-T

79013192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410572-C-G

79013203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410583-C-T

79013336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410712-C-G

79013336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410712-C-T

http://identifiers.org/hco/10/GRCh38#79013438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25410900-C-A

79013449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25410909-A-G

http://identifiers.org/hco/10/GRCh38#79013561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25410996-A-C

79014331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411705-G-A

79014394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411775-C-T

79014398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25411779-C-T

http://identifiers.org/hco/10/GRCh38#79014837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25412110-A-C

79014837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412110-A-G

79015003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412268-A-G

79015145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412396-A-G

79015560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412771-T-G

79015660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412868-A-T

79015797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25412989-T-C

79016364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413717-G-T

79016662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25413906-G-A

http://identifiers.org/hco/10/GRCh38#79016957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25414182-A-C

79017674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25414413-C-G

79017905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25414624-T-A

79018038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25414748-G-A

79018225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25414930-A-G

http://identifiers.org/hco/10/GRCh38#79018374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25415073-C-A

79018374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25415073-C-T

79019822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25417276-T-C

79020021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25417475-T-C

79020106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25417552-G-A

79020136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417589-G-A

79020136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417589-G-C

79020136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417589-G-T

79020241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417683-G-T

79020250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417692-C-T

79020587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25417970-T-C

79020694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25418065-C-T

79020835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25418202-T-G

79021628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418969-C-T

http://identifiers.org/hco/10/GRCh38#79021640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25418981-C-A

79021640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25418981-C-T

79021733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419053-T-C

79021741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419061-C-T

79022015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419294-C-T

79022069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419328-C-T

79022179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419431-G-T

79022189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419450-A-T

http://identifiers.org/hco/10/GRCh38#79022201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25419462-C-A

79022254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419513-G-A

79022254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419513-G-C

79022931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419758-G-A

79023110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419927-C-G

http://identifiers.org/hco/10/GRCh38#79023139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25419956-C-A

79023139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419956-C-T

79023174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25419988-C-T

79023391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420238-G-T

79023459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420292-C-G

79023809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25420631-G-C

79024518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421304-G-C

79024670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421436-C-T

79025056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421745-G-A

79025206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421888-G-A

79025326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25421995-C-T

79025344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25422016-G-T

79025356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25422028-C-T

79025621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25422287-C-T

79026227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423355-C-T

79026276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423422-C-T

79026451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423647-T-A

79026451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423647-T-C

79026541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423816-G-T

79026616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423888-G-C

79026744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25423989-G-A

79027085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424270-C-G

79027141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424314-C-T

79027452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424533-G-A

http://identifiers.org/hco/10/GRCh38#79027520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25424585-C-A

79027627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424687-G-A

http://identifiers.org/hco/10/GRCh38#79027680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25424740-C-A

79027680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424740-C-T

79027687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424746-G-A

79027817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424879-C-G

79027817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25424879-C-T

79028087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425124-C-T

79028182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425224-T-C

http://identifiers.org/hco/10/GRCh38#79028193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25425235-C-A

79028309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425348-G-A

79028445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425470-A-G

79028448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425473-G-A

79028590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425593-C-T

http://identifiers.org/hco/10/GRCh38#79028618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25425621-A-C

79028638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425641-G-A

79028683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425688-G-A

79028686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425691-A-G

http://identifiers.org/hco/10/GRCh38#79028891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25425893-C-A

79028923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25425912-T-C

79030740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25426811-T-C

79031876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25428296-C-T

79034861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431154-C-T

79035004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431288-G-A

79035073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431355-G-C

79035197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431459-C-T

79035225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431485-G-A

79035251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431510-G-A

79035251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431510-G-T

79035326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431606-A-G

79035479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25431752-T-C

79035749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432005-T-A

79035758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25432014-T-A

79043967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438828-G-T

79044048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438910-T-A

79044048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438910-T-C

79044090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438942-C-T

79044104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438959-G-A

79044104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438959-G-T

79044108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438963-G-C

79044108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25438963-G-T

79044214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439033-G-T

79044245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439057-G-T

79044333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439126-T-C

79044403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439268-G-A

79044403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439268-G-T

79044435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439302-C-T

79044498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25439383-T-C

79044526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439409-T-C

79044551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439435-A-G

79044710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439628-A-T

79044753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439685-G-C

79044761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439693-G-A

79044792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25439724-T-C

79046476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441425-A-G

79046684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441664-A-G

79046735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441818-C-T

http://identifiers.org/hco/10/GRCh38#79046791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25441909-C-A

79046838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25441948-G-A

79046888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442001-T-C

79047125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442138-G-C

http://identifiers.org/hco/10/GRCh38#79047264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25442252-C-A

http://identifiers.org/hco/10/GRCh38#79047336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25442323-C-A

79047336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442323-C-G

79047336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442323-C-T

79047393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442369-T-C

79047613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442537-G-C

79047636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442560-C-T

79047762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442696-T-G

79047780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442715-T-C

79047797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442732-T-C

79048001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25442909-C-T

79048211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443076-A-T

79048552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443427-C-G

79048578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443469-C-T

79048743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443677-T-C

79048760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443695-T-C

79048760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443695-T-G

http://identifiers.org/hco/10/GRCh38#79048773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25443733-C-A

79048866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443830-G-A

79048866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443830-G-T

79048874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443841-G-T

http://identifiers.org/hco/10/GRCh38#79048905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25443876-C-A

79048905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443876-C-T

79048923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443895-G-A

79048923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443895-G-C

79048923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25443895-G-T

79049013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443955-T-C

79049020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443963-G-A

79049020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443963-G-T

79049031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443974-T-C

http://identifiers.org/hco/10/GRCh38#79049038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25443981-C-A

79049038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443981-C-T

http://identifiers.org/hco/10/GRCh38#79049039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25443982-C-A

79049039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443982-C-G

79049039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25443982-C-T

79049387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444265-G-A

79049426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444286-C-T

79049541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444385-A-G

79050028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25444542-G-C

79052088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445468-C-T

79052105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445485-G-C

79052146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445523-C-T

79052320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445726-T-C

79052368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445774-C-T

79052435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445824-G-A

79052435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25445824-G-T

79052872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446204-T-C

79052986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446315-G-A

79053111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446420-C-T

79053112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446421-G-A

79053220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446505-G-C

79053433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446693-G-A

79053487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446742-C-T

79053748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25446956-G-A

79053912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447117-G-C

79054094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25447296-G-A

79054424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25447567-G-A

http://identifiers.org/hco/10/GRCh38#79054446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#25447581-C-A

79054585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447709-T-C

79054588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25447712-G-A

79054588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 25447712-G-T

79054590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447714-T-C

http://identifiers.org/hco/10/GRCh38#79054655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25447768-C-A

79054655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25447768-C-T

79054695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25447810-T-A

79054695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25447810-T-C

79054802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25447885-A-G

79056084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448359-C-T

79056397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448666-T-C

79056440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448703-A-G

79056514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448784-C-T

79056632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448865-T-C

79056749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25448977-G-A

79056809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449025-G-C

79056883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449097-C-T

79056986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449233-T-C

79057066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449313-C-T

79058111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449633-G-A

79058134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449655-G-A

79058369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25449874-T-C

79058821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451005-T-C

http://identifiers.org/hco/10/GRCh38#79058831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25451015-C-A

79058831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451015-C-T

79058918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451134-T-C

79059444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25451762-A-G

79059492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451806-C-T

79059607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25451958-T-C

79060590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25452832-C-T

79060591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25452833-G-A

http://identifiers.org/hco/10/GRCh38#79060793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25453045-C-A

79060994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453265-C-G

79060994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453265-C-T

79061045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453315-T-G

79061395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453585-C-T

79061414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453599-G-A

79061565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453754-C-T

79061909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453982-G-A

79061909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453982-G-C

79061909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25453982-G-T

79061969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454039-G-A

79061969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454039-G-T

79062202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454257-G-A

79062202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454257-G-C

79063006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454701-G-A

79063219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454878-G-A

79063252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454914-T-A

79063269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25454931-C-T

79063414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455053-T-C

79065077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455836-C-T

79065195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25455915-C-T

79065802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25456444-A-G

79065820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 25456462-C-T

79065928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25456583-A-G

79066242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25457045-T-C

79066544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25457331-G-A

79066544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 25457331-G-T

79066571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25457358-G-A

79066571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 25457358-G-T

79066781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 25457564-C-T

http://identifiers.org/hco/10/GRCh38#79067406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25458187-C-A

79067533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458304-G-A

http://identifiers.org/hco/10/GRCh38#79067590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#25458355-A-C

79067627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458392-G-A

79067632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458397-T-C

79067690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458446-G-A

79067690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458446-G-T

79067851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27433
most severe consequence: non coding transcript exon variant
orthologous variants: 25458596-G-T