100708726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123240422-G-A

100708765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123240457-C-T

100708785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123240475-T-G

100708879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123240556-A-G

100708953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123240623-C-T

100714664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123241275-C-T

100715050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123241672-C-T

100715509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242360-G-A

100715652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242503-T-C

100715703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242548-C-T

100715786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242622-C-T

100715828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242651-C-T

100715838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242658-C-T

100715859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123242669-A-G

100716679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246046-G-T

100716887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246222-G-A

100716941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246312-G-A

100716941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246312-G-C

100716953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246324-C-T

100717107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246478-G-A

http://identifiers.org/hco/13/GRCh38#100717140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123246511-C-A

100717443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123246821-T-C

100717824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123247515-A-G

100721816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249155-T-C

100721997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249275-G-A

100721997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249275-G-T

100722191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249468-C-T

100722543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249805-T-C

100722556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123249814-T-C

http://identifiers.org/hco/13/GRCh38#100722561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123249819-C-A

http://identifiers.org/hco/13/GRCh38#100722914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123250123-C-A

100722914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123250123-C-T

100722931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123250139-A-G

http://identifiers.org/hco/13/GRCh38#100725140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123252015-C-A

100725153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252042-C-G

100725177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252066-T-C

100725513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252333-A-G

100725754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252559-G-A

100725938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252687-C-T

100725944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252693-A-G

100725976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123252701-A-G

100726706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123255899-G-T

100726758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123255948-G-T

100727402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123256246-T-A

http://identifiers.org/hco/13/GRCh38#100727420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123256264-C-A

100727420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123256264-C-T

100727522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123256360-A-G

http://identifiers.org/hco/13/GRCh38#100746623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123259983-C-A

100746623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123259983-C-G

100746623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123259983-C-T

100746631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123259991-A-G

100746691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123260045-A-G

100746865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123260225-G-T

100747605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123260949-A-G

100747611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123260955-T-A

100747620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123260965-G-C

100747728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261054-C-G

100747728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261054-C-T

100747787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261087-A-T

100748280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261520-G-T

100748315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261551-G-C

100748450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261660-G-A

100748450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261660-G-C

100748464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261673-T-C

100749043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261987-G-C

100749047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123261991-C-T

100749981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123263521-G-T

http://identifiers.org/hco/13/GRCh38#100750177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123263683-C-A

100750177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123263683-C-T

100750231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123263739-C-T

100750426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123264197-G-T

100751306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265183-C-G

100751398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265274-G-A

100751398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265274-G-T

100751404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265280-G-A

100751614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265472-G-A

100751662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123265522-G-A

100752168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123266002-G-A

100753310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123267317-C-T

100753417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123267437-C-G

100753447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123268414-C-G

100753487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123268463-A-G

100753585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123268571-A-G

http://identifiers.org/hco/13/GRCh38#100753587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123268573-C-A

100753587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123268573-C-T

100753961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123268969-C-T

100754151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123269158-G-A

100764545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123270272-G-A

http://identifiers.org/hco/13/GRCh38#100764715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123270448-C-A

100764774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123270520-T-A

100765094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123270803-A-G

http://identifiers.org/hco/13/GRCh38#100765129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123270833-C-A

100765595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123271269-T-A

100765646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123271306-G-C

100765663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123271322-G-A

100765687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123271341-G-A

100765811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123271529-T-C

100765975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123272452-T-C

100765996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123272477-G-A

100766101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123272574-T-C

100767445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123273008-C-G

100768554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275169-G-A

http://identifiers.org/hco/13/GRCh38#100768625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123275240-C-A

100768625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275240-C-G

100768734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275350-G-A

100768784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275400-G-A

100768784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275400-G-T

100768841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275440-T-A

http://identifiers.org/hco/13/GRCh38#100769814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123275900-A-C

100769814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123275900-A-G

100769968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123276024-T-A

http://identifiers.org/hco/13/GRCh38#100770290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123276306-A-C

100770345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123276372-G-C

100770439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123276508-C-T

http://identifiers.org/hco/13/GRCh38#100770488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123276549-A-C

100771317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123276985-G-A

100771454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277057-T-C

100771619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277180-T-C

100772003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277461-G-C

100772243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277533-T-C

100772294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277584-A-G

http://identifiers.org/hco/13/GRCh38#100772315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123277605-C-A

100772315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277605-C-G

100772458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277761-G-T

100772628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277925-G-A

100772628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123277925-G-T

100772703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123278006-T-C

100772804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123278107-G-A

http://identifiers.org/hco/13/GRCh38#100772922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123278240-A-C

100772925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123278243-T-C

100773721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123279065-C-T

100774831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123281191-T-C

100775355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123281223-C-G

100775405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123281272-T-C

100780582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283406-A-G

100780700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283523-G-T

100780736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283541-T-C

http://identifiers.org/hco/13/GRCh38#100780835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123283621-A-C

100780835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283621-A-G

100780860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283637-A-G

100780954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123283824-C-T

100781413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284308-C-T

100781437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284332-G-T

100781633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284438-C-T

100781731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284537-T-C

100781806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284607-T-G

100782757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284727-C-T

100782933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123284887-A-T

100782998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123285313-T-A

100783254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123285558-G-A

100783607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123285826-G-T

100783720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123285939-A-T

100788902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123289266-T-A

100789040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123289408-G-T

100789971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123289915-C-G

100797867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123293476-G-T

100797918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123293990-A-G

100798059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123294131-G-T

100798273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123294350-G-T

100800203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123295394-C-G

http://identifiers.org/hco/13/GRCh38#100800248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123295438-A-C

100800299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123295488-G-C

100800299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123295488-G-T

100800337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123295523-C-T

100800412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123295592-C-G

100803178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123296210-C-T

http://identifiers.org/hco/13/GRCh38#100803265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123296277-A-C

100803265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123296277-A-G

100803318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123296330-A-T

http://identifiers.org/hco/13/GRCh38#100803408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123296410-C-A

http://identifiers.org/hco/13/GRCh38#100803452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123296452-A-C

100803452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123296452-A-T

100807244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123297751-T-G

100807299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123297778-T-C

100807480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123297903-T-A

http://identifiers.org/hco/13/GRCh38#100807570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123297994-C-A

100807974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123298428-A-T

100808495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123300033-C-T

100808704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123300383-G-T

100808720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123300399-G-A

100808861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123300536-A-G

100812298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123303335-G-A

http://identifiers.org/hco/13/GRCh38#100812381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123303418-C-A

100812381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123303418-C-T

http://identifiers.org/hco/13/GRCh38#100814896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123311553-A-C

100814896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311553-A-G

100814902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311562-A-G

100814902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311562-A-T

100814917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311575-T-C

100814975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311636-C-T

100815023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123311680-C-T

http://identifiers.org/hco/13/GRCh38#100815025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123311682-C-A

100815570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123312444-A-G

http://identifiers.org/hco/13/GRCh38#100815591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123312494-C-A

http://identifiers.org/hco/13/GRCh38#100815635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123312546-C-A

100815733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123312629-C-G

100815733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123312629-C-T

100815849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123312723-C-T

100816016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123312882-G-T

100816221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123313031-G-A

100816264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123313075-C-T

100816330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123313138-T-A

http://identifiers.org/hco/13/GRCh38#100816403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123313209-A-C

100818610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123319329-G-A

100819099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123319841-G-A

100819099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123319841-G-C

100819102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123319844-A-G

100819255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123319990-T-C

100819819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123320518-A-G

100821002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123327417-C-G

100821200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123327609-A-G

100821213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123327622-C-G

100821427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123327783-G-C

100822274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328177-A-T

http://identifiers.org/hco/13/GRCh38#100822290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123328193-A-C

100822429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328328-A-G

100822863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328883-A-G

100822922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328941-C-T

100822946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328965-G-A

100822971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123328990-C-T

100823084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329249-G-A

100823167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329332-T-G

100823255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329418-C-T

100823563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329659-C-T

100823614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329699-A-G

100823717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329794-G-A

100823864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329947-G-A

100823864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123329947-G-T

100824056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330178-A-T

100824070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330192-A-T

100824131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330245-G-A

100824161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330273-T-A

100824176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330295-C-T

100824322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330451-G-C

100824345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330473-T-C

100824526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330683-T-C

100824723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330824-G-A

100824724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123330825-T-A

100825111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123331420-G-C

100825111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123331420-G-T

100825489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123331964-T-C

100825494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123331969-C-T

100825517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123331992-T-C

100825667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123332138-G-C

100825723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123332187-A-G

100825757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123332221-A-T

100826167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123333436-A-G

100826264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123333528-A-G

100826283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123333548-T-G

100827586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334171-G-A

100827614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334199-T-C

100827650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334235-G-T

100827653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334237-G-A

100827866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334448-G-A

100828010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334592-A-G

100828181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334757-G-C

100828228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334804-C-G

100828228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334804-C-T

100828243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123334819-C-T

http://identifiers.org/hco/13/GRCh38#100828504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123335055-C-A

100828575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123335128-G-C

100828872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123335411-G-A

100828927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123335461-G-A

100829157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123335880-G-C

100829220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123335983-C-T

100829351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123336068-G-T

100829410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123336111-G-A

http://identifiers.org/hco/13/GRCh38#100829555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123336250-C-A

100829645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123336338-T-A

100833559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123337521-C-T

100833566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123337527-G-T

100833699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123337640-G-A

100834014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123337952-C-T

100834044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123337978-A-T

http://identifiers.org/hco/13/GRCh38#100834335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123338267-C-A

100834335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123338267-C-T

100834434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123338334-G-T

100834462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123338362-G-T

100834584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123338469-C-T

100834889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123338750-C-T

http://identifiers.org/hco/13/GRCh38#100835122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123345758-C-A

100835247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123345882-T-C

100835652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123345937-A-G

http://identifiers.org/hco/13/GRCh38#100835655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123345940-A-C

100837110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347183-A-G

100837136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347205-G-T

100837211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347268-T-C

100837241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347299-T-A

100837321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347383-T-C

http://identifiers.org/hco/13/GRCh38#100837329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123347391-A-C

100837329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347391-A-G

100837465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347684-T-A

100837490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347709-C-T

100837526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347735-G-T

100837691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347852-A-G

100837691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347852-A-T

100837730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347884-G-C

100837769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123347923-G-A

100837862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348017-A-G

100837951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348091-C-T

100838113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348235-T-C

100838212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348334-C-G

100838469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348598-C-G

100838534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348671-C-T

100838723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348941-G-A

100838777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123348988-G-T

100838794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349007-G-A

100838833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349047-C-T

100838848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349076-G-A

100838887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349123-G-A

100839014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349254-A-G

100839404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349340-A-T

http://identifiers.org/hco/13/GRCh38#100839421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123349357-C-A

100839421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349357-C-G

100839443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349372-C-T

100841446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349417-C-T

100841724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123349668-T-C

100842044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350200-G-A

100842044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350200-G-T

100842154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350315-T-C

100842376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350522-G-A

100842415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350560-G-A

100842538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350681-T-C

100842700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123350844-G-A

http://identifiers.org/hco/13/GRCh38#100842729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123350873-C-A

100842913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123351055-A-G

100844680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123352833-A-G

100844680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123352833-A-T

100845315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123353139-C-T

100845399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123353219-G-A

100845399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123353219-G-T

100845419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123353238-G-A

100845654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123353462-G-A

100845915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354104-C-G

100845989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354171-T-C

100846062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354241-G-C

100846490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354316-A-T

100846513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354339-G-A

100846551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354372-C-T

100846560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354397-C-T

100846598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354473-G-A

http://identifiers.org/hco/13/GRCh38#100846741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123354676-C-A

100846741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354676-C-G

100846769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123354725-A-G

100847619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123356832-C-T

100847732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123356927-T-C

100847860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123357039-T-C

100848161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123357682-G-A

100848312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123357790-G-A

100848749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123358229-A-G

100848915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123358405-C-T

100849088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123358573-A-G

100849281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123358689-C-T

100849291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123358699-G-T

100849903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123370403-A-G

http://identifiers.org/hco/13/GRCh38#100849916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123370416-C-A

100849931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123370442-C-T

100850775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123371080-G-A

100850844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123371124-A-G

http://identifiers.org/hco/13/GRCh38#100851037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123371335-A-C

100851364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123371624-G-T

http://identifiers.org/hco/13/GRCh38#100851801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123372503-A-C

100852045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123372710-C-T

100852200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123372844-G-A

100852480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123373123-T-C

100852609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123373255-C-T

100853053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123373764-T-C

100853094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123373808-C-T

100853654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123376383-T-C

100853844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123376569-C-T

http://identifiers.org/hco/13/GRCh38#100854883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123377581-A-C

100854883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123377581-A-G

100855075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123377801-G-C

http://identifiers.org/hco/13/GRCh38#100855161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123377894-C-A

100855459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123378220-T-G

100855513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123378263-C-T

100855519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123378269-T-C

100857693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379078-A-G

100857946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379286-G-A

100857955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379308-C-T

100858218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379578-A-G

100858718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379779-A-T

100858769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123379840-G-A

100859334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123380419-T-C

100859364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123380449-G-A

100859588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123380650-C-G

100859683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123380744-C-G

100859764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123380825-G-A

100860023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123381097-G-A

100860235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123381307-G-C

100869892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123382187-A-G

100869992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123382290-T-A

100870920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123383204-A-G

100871231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123383537-G-A

100871936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123384163-C-G

100876069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123389512-G-A

100876160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123389587-T-A

100876488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123389854-G-A

100876577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123389964-T-G

100876948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123390275-G-T

100877079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123390408-G-C

100877184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123390486-G-A

100877790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123391077-T-C

100878040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123391292-T-C

100878908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123391915-C-T

100878988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123392014-T-A

100878988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123392014-T-C

100878995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123392021-C-T

100879074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123392183-A-G

100880693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394731-A-T

100880778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394817-C-T

100880836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123394875-A-G

http://identifiers.org/hco/13/GRCh38#100881008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123395044-C-A

100881024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395060-T-C

100881182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395216-T-G

100881183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395217-T-C

100881341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395449-T-A

100881719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395850-C-T

100881797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123395927-T-C

100881894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396061-G-C

100881946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396111-A-G

100881946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396111-A-T

100882020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396182-A-G

100882044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396202-C-T

100882146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396272-G-A

100882168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396294-C-T

100882169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123396295-A-G

100883080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399470-T-G

100883137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399554-G-A

100883201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399719-A-G

100883255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123399803-G-A

http://identifiers.org/hco/13/GRCh38#100883428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123399999-A-C

100883658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123400523-C-T

100883786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123400643-T-C

100883927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123400777-C-T

100884197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123401445-G-A

100884571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123401821-C-T

100884836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123402038-C-T

100885616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123403493-T-G

100886349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123404280-A-T

100886362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123404293-T-C

100887137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123405834-G-A

100893391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123406879-A-G

100893469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123406959-G-C

100893469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123406959-G-T

100893558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407053-C-T

100893627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407119-C-G

100893681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407167-C-T

100893943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123407415-G-A

100894416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408104-G-A

100894417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408105-C-G

100894453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408141-G-A

100894457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408145-T-C

100894771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408441-G-A

100894771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408441-G-T

100894943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123408613-G-A

100895123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411705-G-C

100895279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123411843-G-A

100897007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123412601-G-A

100912968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123416382-C-T

http://identifiers.org/hco/13/GRCh38#100913244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123416628-C-A

100913434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123416808-A-G

100913506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123416874-G-A

100913532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123416904-G-A

100913549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123416923-A-G

100913743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123417059-T-A

100914039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123417313-T-C

100914282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123417547-C-T

100914478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123417714-G-A

100914487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123417723-G-A

100915164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418280-G-A

100915241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123418368-G-C

100916970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123421397-A-G

100917088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123421518-C-T

100917118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123421549-C-T

100917150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123421582-A-G

100917704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422284-A-G

100917806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422413-A-G

100917842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422442-T-C

100918062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422610-G-C

100918066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422614-G-A

100918066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123422614-G-C

100918530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423341-G-A

100918592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423401-G-T

100918765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423539-T-C

100918992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423732-A-G

100919023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423761-G-A

100919023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423761-G-T

100919128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423868-A-G

100919128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123423868-A-T

100919570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424296-T-C

100919654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424381-G-A

100920139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424868-T-C

100920290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123424999-T-C

http://identifiers.org/hco/13/GRCh38#100920419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123425129-C-A

http://identifiers.org/hco/13/GRCh38#100920508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123425217-C-A

100920656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123425363-A-G

100922118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123426534-G-C

100922506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123426884-T-C

100922686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123427032-T-C

100924375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123427532-A-G

100924500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123427631-G-A

100924500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123427631-G-T

100932219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430215-C-T

100932541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430559-C-G

100932600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430616-G-C

100932600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430616-G-T

100932779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430788-T-C

100932827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123430836-C-T

100933021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123431046-T-G

100933070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123431095-C-T

100933700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123431635-G-A

100934230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123431970-T-G

100934294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123432028-T-C

100934399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123432130-T-A

100934494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123432234-G-T

http://identifiers.org/hco/13/GRCh38#100935262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123432957-C-A

100935318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433012-C-T

100935328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433020-T-C

100935721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433469-C-T

100935757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433514-C-T

100935765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433522-G-A

100935814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123433572-A-G

100938325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123436285-C-G

100938794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123436419-G-T

100938905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123436508-C-T

100939369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123436947-T-C

100939460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123437037-C-T

http://identifiers.org/hco/13/GRCh38#100940412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123439281-A-C

100940580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439462-G-A

100940710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439586-A-T

100940775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439652-G-C

100940775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439652-G-T

100940878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439763-C-T

100940928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123439813-T-C

100941138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 123440021-G-T

100941149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440032-T-C

100941155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440038-G-A

100941333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440208-C-T

100941368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440243-A-G

100941664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440541-G-A

100941703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123440806-G-T

100942117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441196-A-G

100942269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441359-G-A

100942294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441388-A-G

100942304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441396-G-A

100942304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441396-G-T

100942384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441967-G-A

100942389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123441972-G-A

100942523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442105-A-G

100943088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442325-T-C

100943229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442497-G-T

100943266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442537-A-G

http://identifiers.org/hco/13/GRCh38#100943374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123442639-C-A

100943404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442669-A-G

100943740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442743-T-A

http://identifiers.org/hco/13/GRCh38#100943830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123442793-C-A

100943912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123442873-A-G

http://identifiers.org/hco/13/GRCh38#100944052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123443028-C-A

100944052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123443028-C-T

100944132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123443085-A-G

100944162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123443111-G-A

100944162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123443111-G-T

http://identifiers.org/hco/13/GRCh38#100944431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123443390-C-A

100944452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123443408-G-C

100944467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123443423-G-T

100944508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123443461-A-G

100944972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123443885-C-T

100945689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123444971-G-A

100945691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123444973-A-G

100945706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123444988-T-C

100946356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123445639-T-C

100946532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123445761-T-C

100946751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123445946-C-T

100946841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446036-C-T

100946969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446175-T-C

http://identifiers.org/hco/13/GRCh38#100946977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123446183-A-C

100947032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446246-G-A

100947163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446388-T-A

100947163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446388-T-C

100947170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446395-C-G

100947170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446395-C-T

http://identifiers.org/hco/13/GRCh38#100947321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123446546-C-A

100950285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446925-T-G

100950325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446964-C-G

100950325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446964-C-T

100950347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123446985-A-G

http://identifiers.org/hco/13/GRCh38#100950355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123447002-C-A

100950363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123447012-G-A

100950562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123447200-C-T

100951190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123447813-G-A

100951210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123447833-C-T

100951442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123448054-G-C

100951486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123448130-G-A

100951665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123448308-C-T

100953038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123449318-C-G

100953061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123449338-G-T

http://identifiers.org/hco/13/GRCh38#100953147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123449412-A-C

100953147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123449412-A-G

100953411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123449539-G-A

100953524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123449654-A-G

100953765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450245-C-G

http://identifiers.org/hco/13/GRCh38#100953819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123450289-C-A

100953819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450289-C-G

100953822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450292-C-T

100953835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450305-T-C

100953835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450305-T-G

100953884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450354-G-A

100953956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450427-C-T

100954104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450570-G-A

100954104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450570-G-C

100954141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450609-T-G

100954171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450650-A-G

100954176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450655-T-C

100954320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450775-A-G

100954358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123450812-C-T

http://identifiers.org/hco/13/GRCh38#100954694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123452186-C-A

100955192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123452646-C-T

100956284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123453347-T-G

http://identifiers.org/hco/13/GRCh38#100956370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123453417-A-C

100956370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123453417-A-G

100956370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123453417-A-T

http://identifiers.org/hco/13/GRCh38#100956886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123453920-C-A

100956886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123453920-C-T

100957044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454053-C-G

100957511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454442-G-A

100957573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454502-G-A

100957598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454522-A-G

http://identifiers.org/hco/13/GRCh38#100957621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123454543-C-A

100957621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454543-C-T

100957626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454548-C-T

100957850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454779-T-A

100958027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123454948-A-G

http://identifiers.org/hco/13/GRCh38#100958189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123455088-C-A

100958189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123455088-C-G

100958189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123455088-C-T

100958322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123455209-C-T

100958365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123455251-T-A

100958622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123456795-T-A

100958745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123456916-G-A

100958745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123456916-G-T

100958797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123456967-G-A

100958953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123457122-A-T

100959534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123457674-A-G

100959722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123457867-C-G

100960071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458178-C-T

http://identifiers.org/hco/13/GRCh38#100960285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123458362-C-A

100960430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458504-C-T

100960528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458601-T-C

http://identifiers.org/hco/13/GRCh38#100960536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123458609-C-A

100960536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458609-C-T

100960543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458616-C-G

100960730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123458728-T-G

http://identifiers.org/hco/13/GRCh38#100977844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123463900-A-C

100978018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123464077-C-T

100978080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123464139-C-T

100978299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123464350-C-T

100978861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123464880-A-G

http://identifiers.org/hco/13/GRCh38#100978870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123464889-C-A

100979034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123465051-A-G

100980506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470001-T-G

http://identifiers.org/hco/13/GRCh38#100980602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123470098-C-A

100980602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470098-C-G

100980619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470127-C-T

100980631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470139-G-T

100980716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470229-T-C

http://identifiers.org/hco/13/GRCh38#100981084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123470586-C-A

100981084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470586-C-G

100981084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123470586-C-T

100981284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472066-A-G

100981446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472236-T-A

100981553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472328-G-A

100981760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472528-G-A

100981836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472578-G-T

100982043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472785-G-A

http://identifiers.org/hco/13/GRCh38#100982093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123472836-C-A

100982093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472836-C-T

100982102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472847-G-A

100982143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472877-G-A

100982154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472888-A-T

100982179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123472912-G-A

100982314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123473453-C-T

100982559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123473754-G-A

http://identifiers.org/hco/13/GRCh38#100982577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123473773-A-C

100982718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123473922-T-C

100983627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123474773-G-A

100983734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123474879-C-T

100984113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123475220-C-G

100984237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123475318-A-G

100984261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123475341-A-G

100984283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123475357-T-C

100984820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123475868-T-C

100985161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476152-A-G

100985385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476375-G-A

100985409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476399-C-T

100985477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476462-A-G

100985508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476486-C-T

100986979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123476714-C-T

100987360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477132-T-G

100988052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477485-G-C

100988052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477485-G-T

100988175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477601-G-A

100988281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123477694-G-A

100988756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123478135-T-C

100988764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123478143-A-G

100988971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123478312-A-G

http://identifiers.org/hco/13/GRCh38#100989020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123478357-C-A

100989020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123478357-C-T

100989288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123478618-T-G

100999006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481463-T-C

100999238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481670-A-G

100999283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481716-T-C

100999362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481793-T-C

100999370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481799-G-C

100999406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481833-G-A

100999548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123481969-A-G

100999963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123482364-T-A

101000173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123482569-C-T

101000764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483450-G-A

101000895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483558-C-G

101000915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483578-A-T

101001070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483713-C-T

101001222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123483855-G-T

101004290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123487184-C-T

101007750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488348-G-A

101007750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488348-G-T

101007937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488539-A-G

101008200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488785-G-A

101008200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488785-G-T

101008206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123488791-C-T

http://identifiers.org/hco/13/GRCh38#101008381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123488890-C-A

101008711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489273-G-A

101008854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489418-C-T

101008925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489471-A-T

101009003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489566-T-C

101009277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489823-T-C

101009730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489942-G-A

101009749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123489961-A-G

101009954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490200-T-C

101010145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490375-C-G

http://identifiers.org/hco/13/GRCh38#101010450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123490673-A-C

101010525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490741-T-C

101010546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490762-T-A

101010546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490762-T-C

101010638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123490823-C-G

http://identifiers.org/hco/13/GRCh38#101011555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123491236-A-C

101011565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491245-G-A

101012031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491668-T-C

101012093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123491725-C-T

101012555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493205-G-A

101012627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493273-G-A

101013020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493362-A-G

http://identifiers.org/hco/13/GRCh38#101013050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123493390-C-A

101013126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493467-G-A

101013126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493467-G-T

http://identifiers.org/hco/13/GRCh38#101013252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123493578-C-A

101013269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123493599-T-A

http://identifiers.org/hco/13/GRCh38#101013315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123493665-C-A

101013315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123493665-C-T

101013318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123493668-G-A

101013318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123493668-G-T

101013375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123493726-G-A

http://identifiers.org/hco/13/GRCh38#101013422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123493773-C-A

101016517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496219-C-G

101016584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496290-G-C

101016652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496356-T-C

101016735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496440-T-C

101016838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496546-C-T

101017030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496738-C-G

101017137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123496844-G-A

101023430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123499513-A-G

101023430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123499513-A-T

101023668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123499740-T-C

http://identifiers.org/hco/13/GRCh38#101023739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123499811-C-A

101023739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123499811-C-G

101024212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502388-G-A

101024247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502423-G-C

101024334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123502512-A-T

101024749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123502935-T-A

101024749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123502935-T-C

101024757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non coding transcript exon variant
orthologous variants: 123502944-A-G

101024997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503744-G-A

101024997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123503744-G-C

http://identifiers.org/hco/13/GRCh38#101025150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#123503859-C-A

101025769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504435-C-T

101026205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123504812-C-T

101036125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506156-G-A

101036125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506156-G-T

101036431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506388-T-C

101036558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123506525-C-G

101037180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507099-G-A

101037674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123507619-C-T

101039414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123509674-G-C

101052011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123512757-G-T

101052043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123512787-C-T

101052096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123512840-G-A

101052248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123512865-C-T

101052281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123512891-G-A

101052516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513126-C-G

101052516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513126-C-T

101052593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513202-A-G

101052958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513248-T-C

101053040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513327-C-T

101053101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513387-G-A

101053318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513584-G-A

101053401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513661-T-C

101053554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513808-T-C

101053560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123513815-T-C

101053759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123514026-G-A

101054022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514291-G-T

101054266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514483-C-T

http://identifiers.org/hco/13/GRCh38#101054325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123514542-C-A

101054356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514573-T-G

101054566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514777-A-G

101054631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514840-T-C

http://identifiers.org/hco/13/GRCh38#101054710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123514928-C-A

101054710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123514928-C-G

http://identifiers.org/hco/13/GRCh38#101054829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123515040-C-A

101054913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123515122-G-T

101055089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123515287-C-G

101055089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123515287-C-T

http://identifiers.org/hco/13/GRCh38#101055105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123515348-C-A

http://identifiers.org/hco/13/GRCh38#101055155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123515442-A-C

101055155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 123515442-A-G

101055203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 123515488-T-C

101055243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 123515530-A-G

101055254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 123515540-A-G

101055325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 123515610-G-A

101055445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 123515730-C-T

101055668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123515959-A-T

101056364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123516602-G-A

101056383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123516625-C-T

http://identifiers.org/hco/13/GRCh38#101056922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123517196-C-A

101056922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123517196-C-T

101056966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123517240-C-T

101057236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123517484-G-A

101057236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123517484-G-T

101057238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123517486-T-C

http://identifiers.org/hco/13/GRCh38#101057242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123517490-C-A

101057242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123517490-C-T

http://identifiers.org/hco/13/GRCh38#101057323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123517565-C-A

101057523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123517729-A-G

101057910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518484-T-A

101057910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518484-T-C

101058023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 123518596-G-T

101058353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518871-G-A

101058353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518871-G-C

101058353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518871-G-T

101058388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518904-G-A

101058388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518904-G-T

101058477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123518991-A-G

http://identifiers.org/hco/13/GRCh38#101058509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123519022-C-A

101058614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123519317-C-T

http://identifiers.org/hco/13/GRCh38#101058643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123519343-C-A

101058669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123519373-T-C

http://identifiers.org/hco/13/GRCh38#101058762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123519437-C-A

101058762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123519437-C-G

101058819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123519489-T-C

http://identifiers.org/hco/13/GRCh38#101059135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#123519793-C-A

101059135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42743
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123519793-C-T