35944138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102016629-G-A

35944138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102016629-G-T

http://identifiers.org/hco/11/GRCh38#35944202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#102016582-C-A

35944202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102016582-C-T

35944234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102016552-G-A

35944234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102016552-G-T

http://identifiers.org/hco/11/GRCh38#35944278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102016507-C-A

35944278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102016507-C-G

35944278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102016507-C-T

35944643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102016207-G-T

35945473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102015469-T-C

35946545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102014665-A-G

35946561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102014639-A-G

35946728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102014471-G-A

35947247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013964-G-A

35947314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013927-G-A

35947679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013583-T-A

35947849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013409-A-G

35947911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013346-C-T

35947976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102013297-A-G

http://identifiers.org/hco/11/GRCh38#35948323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102012932-C-A

35948879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012504-A-G

35948988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012439-T-A

35949007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012428-C-T

35949112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012357-T-C

35949176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012302-T-C

35949379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102012093-G-A

35950030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102011487-G-A

35950071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102011449-G-A

35950085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102011435-G-A

35950280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102011265-G-T

35950503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102011116-G-A

35951268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102010105-T-C

35951602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009797-G-C

35951612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009787-A-G

35951781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009442-C-G

35951781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009442-C-T

35951879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009356-C-T

35951882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009353-C-T

35951885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009347-C-T

35951886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009346-C-T

35951910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009341-T-C

35951997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009263-T-C

35952139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009172-A-T

35952140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102009171-T-C

35952665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102007518-T-G

35952840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102007339-A-G

35952990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102007191-G-C

35953005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102007177-T-G

35953132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102007052-A-G

35953264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102006925-G-A

35953515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102006695-A-G

35953800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102006416-G-A

35954195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102006024-G-C

35954450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102004569-A-T

35954812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102004203-T-C

35955674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102003638-T-C

35955677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102003635-C-G

35955704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102003430-A-G

35955717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102003358-A-T

http://identifiers.org/hco/11/GRCh38#35955769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102003246-A-C

35955913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102003113-C-T

http://identifiers.org/hco/11/GRCh38#35956048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102002977-C-A

35956048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102002977-C-T

http://identifiers.org/hco/11/GRCh38#35959123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102002251-C-A

35959123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102002251-C-T

35959169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102002212-A-G

35959209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102002186-A-G

35959304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102002099-G-C

35959383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102001864-T-C

http://identifiers.org/hco/11/GRCh38#35962652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#102000829-A-C

35962788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102000696-A-G

35963709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102000234-C-T

35964084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101999994-A-G

35965349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998848-A-G

35965350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998847-C-T

35965383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998813-G-A

35965526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998699-T-C

35965604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998646-G-T

35965620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101998630-A-T

http://identifiers.org/hco/11/GRCh38#35965686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101998581-C-A

35969221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101997409-C-G

35969579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101997048-G-A

35969624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101997002-C-T

35969667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996953-C-T

35969703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996921-C-T

35969911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996696-T-C

35969981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996633-T-C

35970000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996614-T-C

35970007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996607-G-A

35970092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996532-C-T

35970185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996458-T-C

35970190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101996453-T-C

35970375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101995639-G-A

http://identifiers.org/hco/11/GRCh38#35971002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101995064-A-C

35972483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101993681-T-A

http://identifiers.org/hco/11/GRCh38#35972520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101993652-C-A

35972520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101993652-C-T

http://identifiers.org/hco/11/GRCh38#35972632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101993512-C-A

35973836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101993000-A-T

35973879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992956-T-G

35973931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992914-C-T

35973967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992883-A-G

35974107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992746-C-T

35974156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992697-T-G

35974442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101992348-A-G

35975326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991414-T-A

35975326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991414-T-C

35975353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991398-C-T

35975488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991284-C-T

35975598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991166-G-A

35975598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991166-G-T

35975708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991095-C-G

35975710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101991093-G-A

35976043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990987-G-A

35976045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990986-G-A

35976045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990986-G-T

35976082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990948-T-C

35976440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990640-A-G

35976540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990573-C-T

35976560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990553-G-T

35976751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990405-C-T

35976841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101990316-T-C

35977218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101989764-C-T

35977457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101989564-G-A

35977498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101989524-T-A

35978273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101987528-T-C

35978369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101987433-G-A

35978562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101987254-G-A

35978775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101987111-G-T

35978781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101987105-A-G

35979014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986900-T-C

35979081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986847-C-G

35979081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986847-C-T

35979105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986823-A-G

35979183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986746-A-G

35979214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986715-A-G

35979545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986455-G-A

35979593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986404-G-A

35979671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986331-G-A

35979687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986315-A-G

35979918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101986091-T-G

http://identifiers.org/hco/11/GRCh38#35979946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101986062-A-C

35980022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101985997-G-C

35980190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101985826-G-T

35980693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101985347-A-G

35980693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101985347-A-T

http://identifiers.org/hco/11/GRCh38#35981185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101984587-C-A

35981185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101984587-C-G

35981185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101984587-C-T

35981503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101984332-A-G

35981569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101984245-T-C

35981890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101983720-G-T

35982003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101983621-G-A

35982301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101983354-C-G

35982301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101983354-C-T

35982508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101983216-C-T

http://identifiers.org/hco/11/GRCh38#35982585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101983160-A-C

35983290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101982818-A-G

35983543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101982559-G-T

35984085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981846-T-A

35984085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981846-T-C

35984110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981820-A-G

35984273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981653-A-G

35984295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981635-C-T

35984299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981631-A-T

35984390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981533-A-T

35984400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981520-G-A

35984407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981513-C-T

35984484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981454-C-T

http://identifiers.org/hco/11/GRCh38#35985445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101981188-A-C

35985445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981188-A-G

35985445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981188-A-T

35985967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981073-G-A

35985987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101981052-A-T

http://identifiers.org/hco/11/GRCh38#35986025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101980997-A-C

35986027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980995-G-A

35986042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980976-A-T

35986049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980969-T-C

35986205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980841-T-A

35986460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980625-A-G

35986819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980258-A-G

35986982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980122-C-T

35986998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980108-C-G

http://identifiers.org/hco/11/GRCh38#35986999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101980107-A-C

35987032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980076-T-C

35987053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101980063-C-T

35990127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101979588-G-A

http://identifiers.org/hco/11/GRCh38#35990456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101979331-C-A

35990456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101979331-C-T

35990645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101979123-G-A

35990660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101979103-C-T

35990663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101979100-G-A

35990723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101979050-C-T

35990921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101978968-C-T

35991318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101978555-A-G

35991567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101978298-T-C

http://identifiers.org/hco/11/GRCh38#35992161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101977713-A-C

35992335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101977318-A-G

35992620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101977047-A-G

35992710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101976959-T-C

35993170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101976533-C-T

35993185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101976512-G-A

35993350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101976088-G-A

35993563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101975871-C-T

35993766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101975665-G-T

35998053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101974260-G-A

35998074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101974248-G-T

35998156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101974179-A-T

http://identifiers.org/hco/11/GRCh38#35998166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101974169-C-A

35998166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101974169-C-G

35998351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101974025-A-G

35998479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101973911-A-G

35998591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101973712-A-G

http://identifiers.org/hco/11/GRCh38#35998634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101973679-A-C

35998999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101973323-C-G

35999062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101973261-T-G

35999210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101973127-C-T

36000913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101972915-A-G

36001082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101972767-G-A

36001095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101972755-T-C

36001135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 101972717-A-G

36001371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101972660-T-C

36001384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101972648-T-C

36001885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101972190-T-A

36001900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101972150-C-T

36002054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971710-G-T

36002264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971504-A-T

36002274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971494-T-A

36002349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971427-C-T

36002352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971424-G-A

36002573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101971217-T-G

36002890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101970604-A-G

36002890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101970604-A-T

36002997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101970516-G-A

36003261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101970259-A-G

36003440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101970070-G-A

36006082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101969635-A-G

36006136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101969586-T-C

http://identifiers.org/hco/11/GRCh38#36006498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101969269-A-C

36006608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101969187-A-G

36006837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101968983-C-G

36007234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101968596-G-A

36007573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101968251-G-A

36007891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101967877-T-C

36007963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101967785-T-C

36008060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101967657-G-A

36008516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101967258-T-C

36008706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101967084-G-A

36009032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966734-T-G

36009050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966714-C-G

http://identifiers.org/hco/11/GRCh38#36009097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101966668-C-A

36009175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966578-T-C

36009200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966560-T-C

36009366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966397-G-A

36009442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101966268-A-G

36009675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101965909-G-A

36009681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101965903-C-T

36009759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101965819-T-G

36009920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965669-T-C

36010030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965565-A-G

36010060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965537-G-A

36010060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965537-G-T

36010112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101965486-T-C

36010142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101965457-T-C

36010148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101965451-C-T

36010171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101965436-A-G

36010521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965108-C-T

36010594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101965041-G-C

36010836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101964796-G-A

36012897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101964238-A-G

36012993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101964134-A-G

36013899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963741-C-T

36014119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963525-G-A

36014301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963342-G-A

36014319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101963324-C-T

36014351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101962543-T-C

36014375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101962519-T-C

36014418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101962471-T-C

36015246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101961697-T-C

36015575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101961348-C-G

36015575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101961348-C-T

http://identifiers.org/hco/11/GRCh38#36015658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101961269-C-A

36016512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101960471-T-G

36016513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101960470-G-A

36016635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101960350-G-T

http://identifiers.org/hco/11/GRCh38#36016653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101960333-A-C

36019118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101959125-G-A

36019158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101959085-C-T

36019242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101959001-A-G

36019356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958900-G-A

36019356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958900-G-C

36019471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958783-C-G

36019556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958683-A-T

36019661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958588-G-A

36019661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958588-G-C

36020009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958258-C-T

36020113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958159-A-G

36020117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101958155-T-G

36020827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101957477-A-G

36020846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101957458-G-C

36021055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101957323-C-T

36021494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101956920-G-A

36021494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101956920-G-T

36021511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101956897-G-A

36022084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101956543-G-A

36023069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101955555-C-T

http://identifiers.org/hco/11/GRCh38#36023986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101954735-A-C

36024218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101954468-G-A

36024243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101954454-A-G

36024735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101954179-T-C

36024810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101954118-G-A

36024838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101954099-T-C

http://identifiers.org/hco/11/GRCh38#36024960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101954026-A-C

36025095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101953893-G-A

36025095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101953893-G-T

36025332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101953666-G-A

36025336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101953662-T-G

36027109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101952862-T-C

36027967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101952002-G-A

36028121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101951844-A-G

36028144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101951823-C-T

36028272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101951703-G-T

36028286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101951690-T-G

http://identifiers.org/hco/11/GRCh38#36028352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101951613-C-A

36028768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101951303-C-G

http://identifiers.org/hco/11/GRCh38#36029600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101950822-A-C

36029907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101950534-T-C

36029910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101950531-C-G

36030136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101950297-G-C

36030427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101950009-G-A

36030503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949942-C-T

36030738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101949787-G-T

http://identifiers.org/hco/11/GRCh38#36030897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101949621-A-C

36031057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949469-T-C

36031071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949455-A-G

36031099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949430-G-T

36031163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949366-A-G

36031223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949315-G-A

36031223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949315-G-T

36031228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949310-A-G

36031311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101949228-C-T

36031698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101948680-G-C

36031725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101948651-T-C

36031740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101948636-G-A

36031804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101948561-G-T

36032236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101948209-A-G

http://identifiers.org/hco/11/GRCh38#36032480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101947951-A-C

http://identifiers.org/hco/11/GRCh38#36033196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101947505-A-C

36033478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101947275-C-T

36033842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946906-G-A

36034009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946779-T-C

36034087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946581-T-G

36034221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946227-T-C

36034237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946218-T-C

36034248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946207-T-C

36034362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946104-T-C

36034393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101946075-G-A

36034657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101945838-T-C

36034709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101945783-T-C

36034769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101945535-C-T

36034843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101945447-G-A

36034853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101945437-G-C

36034967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101945284-C-T

36034983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101945268-C-T

http://identifiers.org/hco/11/GRCh38#36035002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101945249-C-A

36035002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101945249-C-G

36035194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101945066-G-T

36035205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101945055-A-G

36035528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944777-A-G

36035557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944744-C-G

36035853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944278-G-T

36035957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944177-A-G

36035987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944149-G-T

http://identifiers.org/hco/11/GRCh38#36035997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101944139-C-A

36035997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944139-C-T

http://identifiers.org/hco/11/GRCh38#36036004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101944132-C-A

36036004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944132-C-G

http://identifiers.org/hco/11/GRCh38#36036034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101944102-C-A

36036034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101944102-C-T

http://identifiers.org/hco/11/GRCh38#36036264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101943863-C-A

36036274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943852-G-C

36036327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943800-G-A

36036327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943800-G-T

http://identifiers.org/hco/11/GRCh38#36036379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101943763-C-A

36036379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943763-C-T

36036398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943744-T-A

36036527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943638-G-A

36036640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943557-A-G

http://identifiers.org/hco/11/GRCh38#36036655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101943543-C-A

36037712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101943121-G-A

36038344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942791-G-A

36038416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942720-T-C

36038614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942531-C-T

36038639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942506-G-A

36038903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942286-A-T

36038904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101942285-G-A

36039854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101940883-T-C

36040426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101940385-C-G

36040515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101940132-C-G

36040515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101940132-C-T

http://identifiers.org/hco/11/GRCh38#36040743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101939793-A-C

http://identifiers.org/hco/11/GRCh38#36040754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101939782-C-A

36040754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101939782-C-T

36040779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101939757-C-T

36040970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101939554-A-T

36041014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101939507-T-C

36041505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101938446-G-C

36041636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101938330-C-T

36041946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101938070-A-G

36042008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101938006-C-G

36042094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937932-A-G

36042178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937877-T-C

36042366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937691-A-T

36042395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937664-G-A

36042446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937649-G-A

36042532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937556-G-A

36042881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101937212-T-G

36043706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101936416-T-C

36044022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101935840-C-G

36044120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101935752-G-A

36044782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101935267-G-A

36044961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101935094-T-C

36045074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101935022-C-T

36045304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934796-A-T

36045428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934680-A-G

36045470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934642-C-T

36046902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934621-T-A

36046959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934569-C-T

36047061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934468-G-A

http://identifiers.org/hco/11/GRCh38#36047065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101934463-C-A

36047085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934445-G-A

36047085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934445-G-T

36047183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934360-G-T

36047333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934168-T-A

36047393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934111-A-T

36047406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101934094-A-G

36047717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933814-A-T

36048018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933532-A-G

36048065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933515-T-G

36048312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933276-G-A

36048327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933252-C-T

36048479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933140-T-C

36048526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101933093-A-G

36048930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932656-C-T

36048963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932628-A-G

36049352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932241-A-T

36049353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932240-A-G

36049368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932225-A-G

36049368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101932225-A-T

36049489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101931357-A-T

36049660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101931239-G-T

36049882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101931027-C-T

36049890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101931019-C-T

36049998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101930923-C-T

36050254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101930377-C-T

36050318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101930309-T-C

36050647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929974-C-G

36050647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929974-C-T

36050703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929940-G-T

36050704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929939-A-G

36050704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929939-A-T

36050711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929932-G-T

36050780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929862-T-C

36050824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929819-C-T

36050886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101929754-C-T

36051002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928753-C-G

36051185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928607-A-G

36051273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928533-C-G

36051474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928338-C-T

36051498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928318-A-G

36051639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101928175-C-T

36052372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101927477-G-A

36052483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101927425-C-T

36052873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926814-C-G

http://identifiers.org/hco/11/GRCh38#36053093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101926616-C-A

36053093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926616-C-T

36053250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926449-T-C

36053289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926411-A-G

36053472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926238-C-T

36053623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926107-C-T

36053647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101926085-G-A

36053912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101925538-C-T

36053999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101925460-C-T

36054173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101925297-C-G

36054178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101925292-C-G

36054266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101925204-A-G

36055212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922948-A-G

36055353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922849-T-C

36055407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922806-G-A

36055476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922737-A-G

36055677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922535-C-G

36055684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922528-C-T

36055735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922461-G-C

36055750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922446-T-G

36055936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922297-T-G

36056404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101922138-C-G

36056559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101922024-G-A

36057231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101921109-G-A

36057242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101921098-T-C

36057508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101920873-C-T

36057577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101920791-T-G

36058246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101919764-C-T

36058429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101919584-G-A

36058447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101919566-T-C

36058909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101919145-G-T

36059756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101917777-C-G

36060942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916759-T-C

36061009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916700-G-A

36061083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916623-T-A

36061083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916623-T-C

36061553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916490-T-G

36061587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916463-A-G

36061906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916164-T-C

36061963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101916107-G-C

36063439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101915355-C-T

36063525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101915273-A-G

36063622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101915170-G-A

36065656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911806-G-A

36065656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911806-G-C

http://identifiers.org/hco/11/GRCh38#36065849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101911655-A-C

36065894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911623-C-G

36065894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911623-C-T

36065916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911602-T-C

36066355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911505-C-T

36066554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911227-T-C

36066604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911174-T-C

36066681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911100-T-C

36066681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911100-T-G

36066685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911096-G-A

36066685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911096-G-T

36066744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101911039-A-G

36066883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910907-C-T

36066958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910825-C-T

36066970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910813-C-T

36067161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910645-G-A

36067172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910634-G-A

36067197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101910614-G-A

36067348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101910496-C-T

36067503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101910404-T-C

36067535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101910373-A-G

36068909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909357-G-A

36069204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909086-C-G

36069246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909045-T-C

36069253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909038-T-C

36069257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909034-G-A

36069279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101909012-C-G

36069329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908980-C-T

36069394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908905-C-T

36069427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908878-C-T

36069492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908813-C-T

http://identifiers.org/hco/11/GRCh38#36069758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101908337-A-C

36069758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908337-A-T

36069895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101908194-C-T

36069910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101908179-C-T

36070137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101907992-T-C

36070291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101907845-G-A

36070531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101907634-T-G

36070650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101907504-G-C

36070833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101906853-G-A

36071170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101906555-G-A

36071338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101906466-A-T

36071465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101906353-T-C

36071480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101906338-A-G

36072035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904797-T-A

36072110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904712-C-T

36072531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904274-C-T

36072579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904212-A-G

36072593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904198-C-T

36072649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101904138-G-T

36080037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101903041-A-G

36080037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101903041-A-T

36080047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101903031-T-C

36080058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101903021-A-G

36080181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902897-T-C

36080335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902746-C-G

36080529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902555-C-G

36080693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902399-A-G

36080751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902340-G-A

36080751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902340-G-T

36080816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902273-A-G

36080819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902270-G-T

36080851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101902248-T-C

36081109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101901711-G-T

http://identifiers.org/hco/11/GRCh38#36081192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101901631-A-C

36081192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101901631-A-G

36081193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101901630-T-C

http://identifiers.org/hco/11/GRCh38#36081281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101901542-A-C

36081281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101901542-A-G

36081281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101901542-A-T

36081427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900640-G-T

36081467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900582-A-G

36081490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900559-C-T

36081534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900525-T-C

http://identifiers.org/hco/11/GRCh38#36081600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101900458-C-A

36081600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900458-C-T

36081624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900431-T-C

36081625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900430-G-A

http://identifiers.org/hco/11/GRCh38#36081631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101900424-C-A

36081676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101900378-C-T

36081797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900264-A-G

http://identifiers.org/hco/11/GRCh38#36081801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101900260-C-A

http://identifiers.org/hco/11/GRCh38#36081909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101900200-C-A

36082007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900117-A-G

36082073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900052-T-C

36082096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101900030-A-G

http://identifiers.org/hco/11/GRCh38#36082162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101899988-C-A

36089943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101894288-C-T

36090079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101894145-C-T

http://identifiers.org/hco/11/GRCh38#36090634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101893615-A-C

36090994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101893300-G-C

36091243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101893090-C-T

36091302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101893055-T-C

36091335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101893025-A-G

36091370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892987-C-G

36091400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892958-G-T

36091571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892826-G-A

36091715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892676-A-G

http://identifiers.org/hco/11/GRCh38#36091808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101892581-C-A

36091820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892569-T-C

36092291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101892184-T-A

36095293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101891449-G-A

36095381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101891367-T-G

36095637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101891124-C-T

36095778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101891012-A-G

36095815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890972-G-T

36095830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890957-A-G

36095854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890933-C-T

36095923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890867-G-T

36095955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890835-G-A

36095992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890800-G-C

36095994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890798-T-C

36096354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890465-C-T

36096450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890380-G-A

36096472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101890358-C-T

36098101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888602-G-C

36098123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888577-C-G

36098124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888576-C-T

http://identifiers.org/hco/11/GRCh38#36098181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101888512-C-A

36098186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888504-A-G

36098213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888479-G-A

36098213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888479-G-T

36098224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888468-T-C

http://identifiers.org/hco/11/GRCh38#36098247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101888456-C-A

36098247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888456-C-G

36098247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888456-C-T

36098269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888440-G-A

36098269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888440-G-T

36098271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888438-G-A

36098271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888438-G-C

36098271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888438-G-T

36098281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888428-G-A

36098281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888428-G-C

36098319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101888392-C-T

36098341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101888370-C-T

36098353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101888358-G-A

36098353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101888358-G-T

36098468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 101888237-A-G

http://identifiers.org/hco/11/GRCh38#36098475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101888225-A-C

36098475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888225-A-G

36098479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888221-T-C

36098603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888133-G-A

36098603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101888133-G-T

36098772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887979-A-G

36098841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887923-T-C

36098884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887880-G-C

36098993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887789-T-C

36099099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887685-A-G

36099099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101887685-A-T

36099719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886912-G-A

36099892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886750-T-C

36100012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886630-G-A

http://identifiers.org/hco/11/GRCh38#36100016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101886626-A-C

http://identifiers.org/hco/11/GRCh38#36100056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101886585-C-A

36100237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886479-C-G

36100414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886320-G-T

36100447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886283-G-A

36100489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101886251-A-G

36101420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885623-C-T

36101473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885573-T-C

36101569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101885482-A-G

36101702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101885369-T-C

36101804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885334-G-A

36101804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885334-G-T

36101845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885293-A-G

36101857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885281-T-C

http://identifiers.org/hco/11/GRCh38#36101860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101885278-C-A

36101860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885278-C-T

36101865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885273-A-G

36102343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101885192-A-G

36103083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101884596-T-C

36103083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101884596-T-G

36103196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101884478-C-G

36104625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101883850-C-T

36104883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883612-T-C

36104894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883600-G-A

36104919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883568-A-T

36105275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883246-T-C

36105283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883238-G-A

36105294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883227-G-A

36105347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101883182-A-G

36105733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101882842-C-G

36105936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101882614-A-G

36109370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101881476-G-A

36109462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101881372-C-T

36109593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101881233-T-A

36109672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101881161-A-G

36109938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101880900-G-A

36109938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101880900-G-T

http://identifiers.org/hco/11/GRCh38#36109939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101880899-C-A

36109974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101880864-T-C

36110268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880545-C-T

36110385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880453-G-T

36110467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880376-G-A

36110543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880322-A-G

36110619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880248-T-A

36110621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880246-G-C

36110646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880221-A-G

36110690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880180-G-A

36110690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101880180-G-C

36110928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879946-G-A

36110928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879946-G-T

36114193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879416-A-G

36114232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879377-C-T

36114266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879347-C-T

36114309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879303-C-T

36114334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879281-T-C

36114452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101879166-T-C

36114721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101878878-C-G

36114886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101878718-C-T

36115703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101877444-A-G

36115703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101877444-A-T

36116195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101877151-T-C

36116254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101877091-C-G

36116445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101876903-G-A

36116497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101876874-C-T

36116500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101876871-T-C

36117395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101876424-G-A

36120138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101872584-C-G

36120167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101872555-G-A

36120364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101872329-G-A

36120559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101872222-G-T

36120637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101872139-G-T

36120932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101871504-C-G

36121348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101871116-G-C

http://identifiers.org/hco/11/GRCh38#36121349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101871115-A-C

36121627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101870844-G-A

36121638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101870833-A-G

36122518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101870021-A-G

36122578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101869974-T-C

36122591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101869961-C-T

36123679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101869139-G-A

36123788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101869030-G-A

36123948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868883-T-C

36124062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868778-G-T

36124376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868465-G-A

http://identifiers.org/hco/11/GRCh38#36124568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101868312-C-A

36124728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868132-G-T

36124747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868111-A-G

36124849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101868045-G-A

36125158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101867773-G-A

36125582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101867393-T-C

36125606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101867352-A-G

http://identifiers.org/hco/11/GRCh38#36125923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101867097-C-A

36125923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101867097-C-G

36126594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101866522-G-A

36126598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101866518-G-A

36126598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101866518-G-C

36126995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101866143-G-T

36127118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865890-T-C

36127365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865559-A-G

36127408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865515-G-T

36127542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865322-A-G

36127596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865124-C-T

36127652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865058-A-G

36127652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865058-A-T

36127707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101865004-G-A

36127719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101864993-G-A

36127825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101864858-C-T

http://identifiers.org/hco/11/GRCh38#36128952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101864164-A-C

36129090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101864034-T-C

36129157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101864001-C-T

36129229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863943-C-G

36129231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863941-A-G

36129391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863794-C-T

http://identifiers.org/hco/11/GRCh38#36129396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101863791-C-A

36129396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863791-C-G

36129597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863561-A-G

36129656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863477-T-C

36129690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863443-A-T

36129927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863296-T-C

36130191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863163-A-G

36130345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101863032-T-A

36130431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101862948-T-C

36130542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101862847-G-A

36131336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101861893-C-T

36131628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101861556-G-C

36131932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101861171-G-T

36132017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101861084-G-C

http://identifiers.org/hco/11/GRCh38#36132070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101861031-C-A

36132070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101861031-C-T

36132199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101860899-G-T

36134051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101858238-T-G

36134086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101858203-A-G

36134501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101857811-C-T

36134848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101857478-T-C

36134854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101857472-C-T

36134944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101857380-G-C

36134956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101857363-C-G

http://identifiers.org/hco/11/GRCh38#36135408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101856955-A-C

36135963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856689-T-C

http://identifiers.org/hco/11/GRCh38#36135977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101856675-C-A

36136049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856604-T-A

http://identifiers.org/hco/11/GRCh38#36136182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101856478-C-A

36136232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856423-C-G

36136255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856397-C-T

36136283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856369-C-T

36137118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856256-T-C

36137269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101856173-T-G

36137644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101855821-C-T

36137803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101855663-T-G

http://identifiers.org/hco/11/GRCh38#36137852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101855614-C-A

36137909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101855567-G-A

36138140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101855346-C-T

36138675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101854848-C-T

http://identifiers.org/hco/11/GRCh38#36139454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101854480-C-A

36139577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101854378-C-G

36139804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101854133-G-A

36139852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101854072-C-T

36140006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101853923-A-G

36140055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101853877-T-G

36140245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101853677-A-G

36140747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101853439-A-G

36140880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101852992-G-A

36140947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101852697-T-C

36141232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101852446-T-C

36141514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101852166-T-C

36141582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101852089-T-C

36141687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101851997-G-A

36142084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101851583-C-G

36142084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101851583-C-T

36143127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101849764-T-C

36143620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101849386-G-C

36147603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848263-C-G

36147684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848187-G-A

36147741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848130-C-G

36147793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848078-A-G

36147823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848050-G-A

36147844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848029-C-G

36147848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848025-T-G

36147901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101848006-C-T

36148254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847909-G-T

36148279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847884-G-A

36148412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847794-G-A

36148412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847794-G-T

36148567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847631-G-C

36148616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847578-G-A

36148680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101847523-C-T

36149430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101846757-G-A

36149430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101846757-G-T

36149662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101846527-G-A

36149663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101846526-C-G

36149818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101846402-G-T

36149992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101846162-G-A

36150040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101846114-A-G

36150215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101845944-T-C

36150572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101845743-T-G

36151012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101845428-T-C

36151240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101845218-G-A

36151481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101844979-C-T

http://identifiers.org/hco/11/GRCh38#36152061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101844479-A-C

36152348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101843590-C-G

36152348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101843590-C-T

36152364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101843572-C-T

36152938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101842782-A-G

36152955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101842765-A-G

36153491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101842224-G-A

36153519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101842196-G-A

36153520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101842195-G-A

36153635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101842102-G-A

36153635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101842102-G-C

36153691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101842047-T-G

36153734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101842004-G-A

36153745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101841993-A-G

36153773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101841965-G-A

http://identifiers.org/hco/11/GRCh38#36153777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101841961-A-C

36153811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101841930-A-T

36154246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101841306-G-A

36154281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101841264-A-G

36154298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101841243-C-T

36154495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840979-G-A

36154613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840889-T-G

36154634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840867-G-A

36155232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840331-A-G

36155266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840296-G-A

36155480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840079-T-C

36155523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101840037-C-G

36156033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839627-C-T

36156074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839610-A-G

36156091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839593-C-G

36156091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839593-C-T

36156136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839533-T-A

36156184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839523-C-T

36156248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839478-T-A

36156553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839224-T-C

36156553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101839224-T-G

36156875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101838918-T-C

36156875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101838918-T-G

36157538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101838267-A-G

36157746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101838056-C-T

36158192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101837179-T-C

36159077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101836504-A-G

36159953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101836297-C-T

36160582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101835717-C-T

36161636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101834925-T-G

http://identifiers.org/hco/11/GRCh38#36162154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101834408-C-A

36162340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101834227-G-A

36162968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101833613-A-T

36163112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101833464-G-A

36163474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101833108-G-T

http://identifiers.org/hco/11/GRCh38#36163490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101833093-C-A

36163649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832959-T-C

36163707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832869-G-T

36163716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832860-G-A

36163716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832860-G-C

36163716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832860-G-T

36163738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832782-A-G

36163753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832767-G-A

36163806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832711-T-C

36163913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832612-T-C

36164194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832356-C-T

36164305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832208-G-A

36164481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101832028-G-A

36164801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101831730-C-T

36164810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101831721-A-G

http://identifiers.org/hco/11/GRCh38#36165077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101831464-C-A

36165614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101830552-T-C

36165934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829956-C-G

36165934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829956-C-T

36166065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829804-A-G

http://identifiers.org/hco/11/GRCh38#36166328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101829540-C-A

36166328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 101829540-C-T

36166579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829326-A-G

36166592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829313-A-G

36166592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829313-A-T

http://identifiers.org/hco/11/GRCh38#36166788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101829118-A-C

36166810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101829096-A-G

http://identifiers.org/hco/11/GRCh38#36167153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101828779-A-C

36167768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827982-T-C

36168284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827465-A-G

36168523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827247-G-C

36168523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827247-G-T

36168550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827220-A-T

36168618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827152-T-C

36168693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101827080-T-G

36168824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826933-T-C

36168925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826831-C-G

36168925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826831-C-T

36168950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826800-G-A

36180343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826143-C-T

36180402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826091-G-A

36180443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826049-T-C

36180471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101826012-G-A

36180586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825897-T-G

36180806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825753-G-A

36180904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825691-T-C

36180961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825639-T-A

36180965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101825635-G-A

http://identifiers.org/hco/11/GRCh38#36181362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101824368-C-A

36181362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824368-C-T

36181438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824293-C-T

36181447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824284-C-T

36181468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824263-G-A

36181473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824258-G-A

36181556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824183-C-G

36181583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101824153-C-T

36181813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823942-A-T

36182072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823701-T-G

http://identifiers.org/hco/11/GRCh38#36182164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101823608-A-C

36182181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823591-C-G

36182445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823410-T-A

36182731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823142-G-C

36182842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101823036-A-T

36182923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822935-A-G

36183005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822857-C-G

36183106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822749-T-C

http://identifiers.org/hco/11/GRCh38#36183111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101822744-A-C

36183172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822683-C-T

36183289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822555-C-T

36183409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101822058-G-T

36183596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101821896-A-G

http://identifiers.org/hco/11/GRCh38#36183763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101821769-C-A

36183917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101821616-T-G

36184638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101821200-T-C

36185245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101820571-A-G

36185520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101820318-G-A

http://identifiers.org/hco/11/GRCh38#36185750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101820086-C-A

36185975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101819866-A-G

36186430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101819479-A-G

36186776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101819162-A-G

36186920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101819025-C-T

36186967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101818978-C-T

36187113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101818826-T-C

36187113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101818826-T-G

http://identifiers.org/hco/11/GRCh38#36187844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101817958-A-C

36188092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817712-A-G

36188099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817705-C-T

http://identifiers.org/hco/11/GRCh38#36188242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101817560-C-A

36188242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817560-C-T

36188466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817384-A-G

36188719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817175-A-G

36188828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817080-C-T

36188935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101817016-A-G

36191786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814456-G-C

36191865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814377-T-C

36192007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814241-A-G

36192231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814019-G-C

36192231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101814019-G-T

36192773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813493-G-A

36192785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813481-C-G

36192842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813433-C-T

36192901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813378-C-T

36193185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813292-G-A

36193191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813286-A-G

36193206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101813271-G-A

36193611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812899-C-T

36193750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812771-G-A

36193752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812769-G-A

36194019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812475-T-C

36194084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812381-C-T

36194299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101812017-A-G

36194455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811891-C-G

36194988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811421-A-G

36195278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811176-T-G

36195303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811151-G-C

36195455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101811028-T-C

36195545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810938-T-C

36195683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101810798-C-T

36196095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809838-C-G

http://identifiers.org/hco/11/GRCh38#36196129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101809804-C-A

36196190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809747-G-T

36196218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101809720-A-G

http://identifiers.org/hco/11/GRCh38#36196264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101809674-A-C

36196435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809504-C-T

36196450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809489-C-T

36196467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809473-T-C

36196510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809422-A-G

36196532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809396-T-C

36196574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 101809354-T-C

36196605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809323-G-A

36196605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809323-G-T

36196676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809261-G-A

36196676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101809261-G-T

36197131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808826-G-T

36197133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808824-G-A

36197133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808824-G-T

36197263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808708-A-T

36197354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808617-G-T

36197366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808605-G-T

36197378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808593-G-T

36197397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808574-C-T

36197445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808505-A-G

36197521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808430-T-C

36197575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808403-T-C

http://identifiers.org/hco/11/GRCh38#36197577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101808401-C-A

36197577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808401-C-T

36197597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808381-C-G

36197597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808381-C-T

36197745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808273-T-C

36197769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101808249-C-T

http://identifiers.org/hco/11/GRCh38#36198441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101807644-C-A

36198441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807644-C-T

36198520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807573-C-T

36198647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807462-C-T

36198714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101807401-A-G

36199498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806943-C-G

36199498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806943-C-T

36199561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806873-G-A

36200296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806507-T-G

36200302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806501-C-T

36200340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806455-C-T

36200346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806449-T-A

36200365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806434-T-A

36200438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806362-C-G

36200537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806274-T-C

36200553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806256-G-T

36200780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101806039-T-G

36201180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804735-A-G

36201259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804662-C-G

36201269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804652-G-T

36201324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804617-T-A

36201676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804285-G-A

36201695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101804266-C-T

36203390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101803427-G-T

36203620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101803237-A-G

36203922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101803040-T-C

36204123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802832-T-C

36204173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802782-A-G

36204250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802702-G-A

36204353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802602-A-T

http://identifiers.org/hco/11/GRCh38#36204371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101802585-A-C

36204385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802573-A-G

36204480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802542-T-C

36204590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802505-C-T

36205008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802325-C-T

36205009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802324-C-G

36205009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802324-C-T

36205028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802305-C-T

36205248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101802078-A-G

36205384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101801935-C-T

36205411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101801905-T-C

36205819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101800750-G-A

36205904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101800671-G-A

36206171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101800408-G-A

36206171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101800408-G-T

36206442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101800034-A-G

36206527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101799946-C-T

36206562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101799919-C-T

http://identifiers.org/hco/11/GRCh38#36206613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101799867-A-C

36209960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101798415-G-A

36210331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101798091-C-G

36210527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101797891-G-A

http://identifiers.org/hco/11/GRCh38#36210639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101797781-A-C

36210644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101797776-T-C

36210688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101797732-A-T

36211103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101797251-G-T

36211447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101796901-G-A

36211447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101796901-G-C

36211846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101796604-T-C

36211858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101796593-C-T

http://identifiers.org/hco/11/GRCh38#36212288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101796198-C-A

36212297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101796193-G-A

36212712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101795811-C-T

36212741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101795786-G-A

36213157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101793949-G-A

36213202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101793909-G-A

36213216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101793903-T-G

36213278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101793845-C-T

36213305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101793814-T-C

http://identifiers.org/hco/11/GRCh38#36213402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101793719-A-C

36214769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792190-G-T

36214812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792168-A-G

36214817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792163-T-G

36214908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792073-C-T

36214955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101792033-C-T

http://identifiers.org/hco/11/GRCh38#36214995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101792002-C-A

36215199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791875-G-A

36215199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791875-G-T

36215528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101791565-G-A

36216314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790854-T-G

36216418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790755-A-G

36219178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790166-T-G

36219200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101790148-G-C

36219739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789692-G-A

36219877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789585-A-G

36219936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789529-A-G

36219955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789510-A-G

36219961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101789504-C-T

36221029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101788980-T-G

36222214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787643-A-G

36222236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787612-T-C

36222441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787359-C-T

http://identifiers.org/hco/11/GRCh38#36222585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101787213-C-A

36222585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787213-C-T

36222779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101787033-G-A

http://identifiers.org/hco/11/GRCh38#36223306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101786524-C-A

36223399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101786433-C-T

36226835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785745-C-T

36226931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785654-G-A

36226937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785648-T-C

http://identifiers.org/hco/11/GRCh38#36226995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101785607-C-A

36226995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785607-C-G

36226995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785607-C-T

http://identifiers.org/hco/11/GRCh38#36226997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101785605-C-A

36226997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785605-C-T

36226998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785604-A-G

36226998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785604-A-T

http://identifiers.org/hco/11/GRCh38#36227066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101785536-C-A

36227366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101785236-G-A

36227381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 101785221-T-C

36227451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785164-A-T

36227479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785140-G-A

36227479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785140-G-T

http://identifiers.org/hco/11/GRCh38#36227501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101785118-C-A

36227503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785116-G-T

36227508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785111-T-A

36227534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785085-T-C

36227546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785073-G-T

36227569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785050-G-A

36227569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785050-G-T

36227627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101785001-G-A

http://identifiers.org/hco/11/GRCh38#36227838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101784880-A-C

http://identifiers.org/hco/11/GRCh38#36228265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101784333-A-C

http://identifiers.org/hco/11/GRCh38#36228421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101784194-A-C

36228679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783971-T-G

36228817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783842-C-T

36229031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783647-G-T

36229046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783634-T-C

36229073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783607-G-A

36229073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783607-G-C

36229087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 101783572-T-C

36229164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 101783514-G-A

http://identifiers.org/hco/11/GRCh38#36229650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101783016-A-C

36229650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101783016-A-G

36229667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782999-G-A

36229667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782999-G-C

36229697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782941-G-A

36229697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782941-G-T

36229732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782911-T-G

36229733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782910-G-A

36229751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782892-A-G

36229771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782872-C-G

http://identifiers.org/hco/11/GRCh38#36229862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782783-C-A

36229862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782783-C-G

36229862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782783-C-T

36229954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782696-G-T

36229960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782690-G-T

36230104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782560-T-C

36230106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782558-A-G

http://identifiers.org/hco/11/GRCh38#36230168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782506-A-C

36230168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782506-A-G

http://identifiers.org/hco/11/GRCh38#36230174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782500-C-A

36230174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782500-C-T

http://identifiers.org/hco/11/GRCh38#36230233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782442-C-A

36230279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782398-G-A

36230279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782398-G-C

36230279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782398-G-T

36230300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782377-G-A

36230300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782377-G-T

36230317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782360-C-T

36230411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782267-G-T

http://identifiers.org/hco/11/GRCh38#36230460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782216-C-A

36230494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782182-A-G

http://identifiers.org/hco/11/GRCh38#36230499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#101782177-C-A

36230499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101782177-C-T

36230788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781886-C-G

36230788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781886-C-T

36230894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781789-G-T

36231001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781697-C-T

36231124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781588-A-G

36231143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781569-A-G

36231181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781531-G-T

36231193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101781519-T-A

http://identifiers.org/hco/11/GRCh38#36231258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#101781464-C-A

36231463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101781252-A-T

36231467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 101781248-G-T

36231794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101780915-C-T

36231805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27046
most severe consequence: 3 prime UTR variant
orthologous variants: 101780902-T-A