105708820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797558-G-C

105708827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797551-G-A

105708827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797551-G-T

http://identifiers.org/hco/4/GRCh38#105708833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#132797545-A-C

105708833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797545-A-G

105708836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797542-A-G

105708890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132797470-G-T

105709092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132797269-G-A

105709092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132797269-G-T

105709113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132797249-A-G

105709197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132797183-C-T

105709199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132797181-T-C

105709258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132797118-C-G

105709258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132797118-C-T

105709298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132797076-A-G

105709604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796774-A-G

105709652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796738-T-C

105709913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796516-T-C

105709943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796490-T-A

105712681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794704-T-C

105712693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794692-T-A

105712693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794692-T-C

105712743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794643-A-G

105712769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794623-G-A

105714099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792675-C-G

105714249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792518-A-G

105714258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792499-C-G

105714260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792497-G-A

105714343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792417-G-A

105714547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792227-A-G

105714610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792168-A-G

105714642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792140-T-C

105714792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132792028-G-T

105714901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132791920-C-T

http://identifiers.org/hco/4/GRCh38#105716370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132791388-C-A

105717297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132791065-A-G

http://identifiers.org/hco/4/GRCh38#105717310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132791051-C-A

105717554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132790824-T-G

105717555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132790823-A-G

105717611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132790766-A-G

105717866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132790508-G-A

105718930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788407-A-G

105718930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788407-A-T

105718943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788394-G-A

105718943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788394-G-T

105718948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788389-G-A

105718948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788389-G-T

105719183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788142-A-G

105719287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788038-G-C

105719432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132787893-G-C

105719437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 132787888-C-T

105719510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132787815-T-C

105719585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787740-A-G

105719597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787728-C-G

105719941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787205-T-A

105720290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132786897-C-T

http://identifiers.org/hco/4/GRCh38#105720563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132786665-A-C

105720946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785471-T-C

105721656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785099-T-G

105721699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785061-A-G

105721702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785059-T-C

105724429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132780754-A-T

105724441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132780741-T-C

105724745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132780444-A-G

105724928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132780275-T-C

105725883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778716-A-G

105726320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778165-G-A

105726557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777930-G-A

105726922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777571-T-G

105726948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777539-T-G

105727087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777459-A-T

http://identifiers.org/hco/4/GRCh38#105728352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132776035-A-C

105728422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132775979-G-A

105729326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768475-A-G

105729433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132768391-C-G

105729433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132768391-C-T

105729493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132768331-A-G

105729532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768286-T-A

105729532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768286-T-C

105729585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768233-G-A

105729585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768233-G-T

105729716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768111-T-C

105740663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767522-T-G

105740757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767434-G-A

http://identifiers.org/hco/4/GRCh38#105740789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132767406-C-A

105740843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767362-C-T

105740847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767358-A-G

http://identifiers.org/hco/4/GRCh38#105740855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132767345-C-A

105740880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767321-A-G

105740915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767307-C-T

105740970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767261-T-C

105742243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765720-A-G

105742375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765593-T-C

105742694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765260-G-T

105742740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765214-G-T

105743179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764760-T-C

105743287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764675-T-G

105745113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764171-A-T

105745312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763986-T-C

105745379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763938-G-C

105745653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763686-G-A

105745655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763684-C-T

105745693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763644-T-C

105746881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763227-C-T

105747169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762897-A-G

105747263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762806-G-C

105747303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762767-A-G

105747324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762746-A-G

http://identifiers.org/hco/4/GRCh38#105747481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132762618-C-A

105747722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762422-G-A

105748488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761817-C-T

105748608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761742-G-T

105748627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761726-T-C

105752302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759298-A-G

105752645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759027-G-T

105752675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759018-T-C

105752919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758826-T-C

http://identifiers.org/hco/4/GRCh38#105753135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132758604-A-C

http://identifiers.org/hco/4/GRCh38#105753306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132758472-A-C

105753306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132758472-A-G

105754029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758120-T-C

105754118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758033-A-T

105754418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757762-A-G

105754503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757685-G-T

105754537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757651-A-G

105756993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756685-G-A

105757154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756536-C-T

105757221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756423-A-G

105757475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756154-A-G

105759048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754802-T-A

105759249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754490-T-A

105759421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754190-G-C

http://identifiers.org/hco/4/GRCh38#105760081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132752586-C-A

105760147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752528-T-A

http://identifiers.org/hco/4/GRCh38#105760167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132752499-C-A

105760167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752499-C-G

105760170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752496-A-G

http://identifiers.org/hco/4/GRCh38#105760196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132752470-C-A

105760351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752332-G-T

105760523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752150-G-A

105761503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132752004-G-T

105761519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751988-A-G

105761662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751844-C-T

105761881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751616-T-G

http://identifiers.org/hco/4/GRCh38#105761977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132751535-A-C

http://identifiers.org/hco/4/GRCh38#105762027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132751487-C-A

105762027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132751487-C-T

105762204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132751345-C-T

105762540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132751054-G-C

105762540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132751054-G-T

105762777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132750830-A-T

105762853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132750760-A-G

105764370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132750205-C-T

105764400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132750175-A-G

105764736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749853-G-A

105764744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749845-G-A

105779697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749458-T-C

105779721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749232-A-G

105779721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749232-A-T

http://identifiers.org/hco/4/GRCh38#105779907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132749067-C-A

105779907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132749067-C-G

105780790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132748271-T-C

105781155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132747955-A-G

105781654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132747819-G-A

105781654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132747819-G-T

105782898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132747434-T-A

105788849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741657-A-G

105789639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132740960-G-C

105792387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739767-G-A

105792954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739291-A-G

105793115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739136-C-T

105793136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739115-T-A

105793302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738970-T-G

105793619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738660-A-G

105793639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738638-G-T

105793712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738584-A-G

105794003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738271-G-A

105794051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738217-G-A

105794192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132738084-T-C

105794411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132737895-G-C

105794645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132737687-C-T

105803794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132734408-A-T

105803955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132734280-T-A

105803963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132734272-T-C

105804135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132734097-T-C

105804364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132733869-A-G

http://identifiers.org/hco/4/GRCh38#105805834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132732787-C-A

105806161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732508-A-G

105806181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732488-G-C

105806291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732379-T-C

105806311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732367-T-C

105806359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732319-G-A

105806359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732319-G-C

105806359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132732319-G-T

105806915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132731792-G-T

105810157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729461-G-A

http://identifiers.org/hco/4/GRCh38#105810301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132729324-A-C

http://identifiers.org/hco/4/GRCh38#105810414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132729196-A-C

105810435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729175-T-A

105810435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729175-T-C

105810489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729125-A-G

105810505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729113-C-G

105810505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729113-C-T

105810509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729109-G-T

105810552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132729043-T-C

105812549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718645-G-A

http://identifiers.org/hco/4/GRCh38#105812613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132718591-C-A

105812614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718590-C-G

105812875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132718331-T-G

105813276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717993-C-T

http://identifiers.org/hco/4/GRCh38#105815732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132717255-C-A

105815739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132717248-C-T

105816154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716883-C-T

105816473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716579-A-G

105816776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716298-A-G

105816924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716176-C-T

105817124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132716001-A-T

105817291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132715815-A-G

105817518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132715567-C-T

105817873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132715458-T-G

105818179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132715155-A-G

http://identifiers.org/hco/4/GRCh38#105818521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132714849-A-C

http://identifiers.org/hco/4/GRCh38#105818679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132714642-C-A

105818830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132714524-T-C

105818919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132714425-T-G

105819483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713983-G-A

105819505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713962-T-C

http://identifiers.org/hco/4/GRCh38#105820049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132713408-A-C

105820217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713291-C-T

105820400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713136-T-G

105820430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713106-T-C

105820494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132713050-G-C

105820582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132712988-G-A

http://identifiers.org/hco/4/GRCh38#105820586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132712984-C-A

105820586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132712984-C-T

http://identifiers.org/hco/4/GRCh38#105820659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132712920-C-A

105820806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712778-A-G

105821991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712547-T-G

105822016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712522-T-C

105822026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712512-T-C

105822363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712259-A-G

105822434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712189-A-T

105822477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132712151-T-G

105822818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711540-A-G

105822843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711515-G-A

105822910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132711473-A-G

http://identifiers.org/hco/4/GRCh38#105823108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132711282-A-C

http://identifiers.org/hco/4/GRCh38#105823266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132711156-A-C

105823266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132711156-A-G

105823266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 132711156-A-T

http://identifiers.org/hco/4/GRCh38#105823446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132711016-A-C

http://identifiers.org/hco/4/GRCh38#105823461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132711001-A-C

105823548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132710922-A-G

http://identifiers.org/hco/4/GRCh38#105823576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132710894-C-A

http://identifiers.org/hco/4/GRCh38#105825612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709617-C-A

http://identifiers.org/hco/4/GRCh38#105825647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709576-C-A

105825647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709576-C-T

105825648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709575-T-C

105825648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709575-T-G

http://identifiers.org/hco/4/GRCh38#105825853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709376-C-A

105825853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709376-C-T

http://identifiers.org/hco/4/GRCh38#105825930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709299-C-A

105825935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709294-A-T

http://identifiers.org/hco/4/GRCh38#105825986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709247-A-C

105825986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709247-A-G

105825986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709247-A-T

http://identifiers.org/hco/4/GRCh38#105825999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709236-C-A

105825999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709236-C-T

http://identifiers.org/hco/4/GRCh38#105826024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132709211-C-A

105826070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709173-T-C

105826135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709145-A-G

105826153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709127-A-G

105826157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709114-A-G

105826197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132709074-A-T

105826340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708946-T-C

105826545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708771-G-A

105826545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708771-G-T

105826625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708692-T-C

105826771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708562-G-C

105827390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132708200-G-A

105834451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704727-T-C

http://identifiers.org/hco/4/GRCh38#105834581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132704597-A-C

105834601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132704579-A-G

105834625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704555-C-G

http://identifiers.org/hco/4/GRCh38#105834648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132704533-C-A

105834648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704533-C-G

http://identifiers.org/hco/4/GRCh38#105834705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132704296-C-A

105834738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704261-G-A

105834738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704261-G-T

105834844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132704176-T-C

105836842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702922-A-G

105837049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702741-A-G

105837069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702718-C-T

105837325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132702487-G-C

105837403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702411-T-C

105837417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702397-G-A

105837427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702371-C-T

105837463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702311-T-C

105837518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702258-A-G

105837620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702188-A-G

105837711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702098-A-T

105837772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702037-G-T

105837790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702017-T-C

105837800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132702007-A-G

http://identifiers.org/hco/4/GRCh38#105837894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132701920-C-A

105837894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701920-C-T

105837911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701899-T-A

105837911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701899-T-C

105837946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701728-T-C

105837952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701722-T-A

105837963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701708-G-T

http://identifiers.org/hco/4/GRCh38#105838029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132701651-C-A

http://identifiers.org/hco/4/GRCh38#105838250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132701457-C-A

105838278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701437-T-C

105838283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701432-C-T

105838303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701415-G-C

105838459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701272-G-A

105838629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701151-G-A

105838712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132701073-A-T

105838796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132700998-T-G

http://identifiers.org/hco/4/GRCh38#105838835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132700964-A-C

105838835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132700964-A-G

105838996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132694624-C-G

105839054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132694564-G-A

105839809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132694347-T-C

http://identifiers.org/hco/4/GRCh38#105839858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132694303-A-C

105839871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132694292-T-C

105840051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132694021-A-G

105840184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132693903-A-G

http://identifiers.org/hco/4/GRCh38#105840362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132693724-C-A

105840433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132693656-A-G

105840461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132693598-A-T

105840956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132693157-A-G

105841051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132693050-C-G

http://identifiers.org/hco/4/GRCh38#105841107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132692972-A-C

105841441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132692723-T-G

105841587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132692576-G-A

105841590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132692573-C-T

105841741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692493-C-G

105841741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692493-C-T

105841755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692477-C-T

105841782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692447-C-T

105842126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132692152-G-A

105842166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692113-T-C

105842183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692096-C-G

105842183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692096-C-T

105842219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692061-T-A

105842219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132692061-T-G

105842375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691951-T-C

105842842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691571-T-C

105843187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691234-G-A

105843346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691112-T-C

105843431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132691025-G-T

105843472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690994-A-G

105843519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132690944-A-G

105843544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132690915-T-C

http://identifiers.org/hco/4/GRCh38#105843561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132690899-C-A

105843619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690853-T-C

http://identifiers.org/hco/4/GRCh38#105843677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132690799-A-C

105843785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690717-A-G

105843790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690712-A-G

105843896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690585-A-G

105843896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132690585-A-T

105844594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689726-T-C

105845029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689364-C-T

105845315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689100-A-T

105845339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689077-A-G

105845339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689077-A-T

105845347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689069-T-C

105845391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689021-T-C

105845399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132689013-T-A

105845589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688832-C-T

105845590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688831-A-G

http://identifiers.org/hco/4/GRCh38#105845605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132688816-C-A

105845605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688816-C-T

http://identifiers.org/hco/4/GRCh38#105845628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132688794-C-A

105845628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688794-C-T

105845634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688788-G-A

105845645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688777-G-A

105845645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688777-G-T

105845695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 132688731-T-C

105845766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688682-G-A

http://identifiers.org/hco/4/GRCh38#105845806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#132688644-C-A

105845842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688607-A-G

105845859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688593-T-C

105845859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688593-T-G

105845886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688576-T-G

105845916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688547-T-G

105845926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688537-G-A

105845926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688537-G-C

105845926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688537-G-T

105845998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688467-T-C

105846063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688402-A-G

105846120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688346-C-T

105846476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688232-G-A

105846536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132688167-A-G

105847101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132687916-G-T

105847313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132687723-A-G

105847333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132687708-T-A

105847416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25806
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 132687631-T-C