85154925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145728223-C-T

http://identifiers.org/hco/1/GRCh38#85156676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145727772-A-C

85156694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145727764-G-A

85156694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145727764-G-C

85156874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145727463-A-G

85156924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145727412-C-T

http://identifiers.org/hco/1/GRCh38#85156951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145727383-C-A

85157398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145727059-T-C

85157688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726779-G-A

85157702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726765-G-A

85157815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726662-C-T

85157879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726597-G-A

http://identifiers.org/hco/1/GRCh38#85158027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145726448-C-A

85158027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726448-C-G

85158027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726448-C-T

85158425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726368-T-C

85158451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726350-G-A

85158451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726350-G-T

http://identifiers.org/hco/1/GRCh38#85158458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145726343-A-C

85158575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726234-G-T

85158730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726078-A-T

http://identifiers.org/hco/1/GRCh38#85158740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145726062-A-C

85158740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726062-A-G

http://identifiers.org/hco/1/GRCh38#85158741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145726061-C-A

85158741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3 prime UTR variant
orthologous variants: 145726061-C-G

http://identifiers.org/hco/1/GRCh38#85158787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145726015-C-A

85158787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145726015-C-T

85158804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 145725998-C-T

85158901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145725901-T-A

85158917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145725885-T-C

85158923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 145725879-G-A

85158942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 145725860-C-T

85158944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145725858-C-T

85158958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145725844-T-C

85159239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 145725566-T-G

85159282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145725521-A-G

85159429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145725385-A-G

85159795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145725046-A-G

85159796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145725045-C-T

85160005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724810-C-T

85160034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724781-C-T

85160039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724776-G-A

85160055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724760-A-G

85160123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724693-A-G

http://identifiers.org/hco/1/GRCh38#85160184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145724625-A-C

85160184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724625-A-G

85160191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724619-T-C

85160297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724544-G-A

85160297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724544-G-T

85160996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724101-A-G

85161017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724080-T-G

85161031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145724066-T-C

http://identifiers.org/hco/1/GRCh38#85161104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145723990-A-C

85161152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145723953-G-T

85161215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145723884-T-C

85161290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145723824-G-C

http://identifiers.org/hco/1/GRCh38#85161303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145723811-A-C

85162138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145723417-C-T

85162596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145723009-T-C

85164019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145722055-C-T

85164120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721976-T-C

85164120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721976-T-G

85164144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721952-A-T

85164218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721880-G-A

85164280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721826-C-T

85164286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721820-T-G

85164392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721719-G-T

85164410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721702-T-A

85164464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721641-T-C

85164482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721623-A-G

85164486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721619-T-C

85164492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721613-T-C

85164501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721604-A-G

85164506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721599-A-G

85164515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721591-G-T

85164520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721586-A-G

85164552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721554-A-G

85164552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721554-A-T

85164597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721509-T-C

85164632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous variant
orthologous variants: 145721474-A-T

85164637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721469-C-T

85164646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: stop gained
orthologous variants: 145721460-G-A

85164646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721460-G-T

85164660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721446-G-A

85164660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721446-G-T

http://identifiers.org/hco/1/GRCh38#85164669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145721437-C-A

85164669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145721437-C-T

http://identifiers.org/hco/1/GRCh38#85164737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145721369-C-A

85165268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721320-A-G

http://identifiers.org/hco/1/GRCh38#85165318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145721276-C-A

85165327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721267-G-C

85165327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721267-G-T

85165398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721207-A-G

85165437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721182-G-A

85165445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145721175-C-T

85168902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720321-G-T

85168906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720317-T-C

http://identifiers.org/hco/1/GRCh38#85168937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145720288-C-A

85169010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720226-G-A

85169010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720226-G-C

85169010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720226-G-T

85169014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720222-T-C

85169032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145720204-G-A

85169069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145720167-A-G

85169283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719959-T-C

85169283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719959-T-G

http://identifiers.org/hco/1/GRCh38#85169306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145719935-A-C

85169306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719935-A-G

85169389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719853-C-T

85169425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719818-G-A

85169659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719610-A-G

85169662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719607-G-A

http://identifiers.org/hco/1/GRCh38#85169670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145719599-C-A

85169670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719599-C-T

85169731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145719525-G-C

85171381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145718116-T-C

http://identifiers.org/hco/1/GRCh38#85171557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145717944-C-A

85171822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145717736-A-G

85172134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145717579-T-C

85172289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145717450-T-C

85172299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145717445-G-A

85172299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145717445-G-T

85175266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 145716158-G-A

85175867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 145715547-A-T

http://identifiers.org/hco/1/GRCh38#85176117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145715304-C-A

85177066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713765-G-C

85177118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713716-G-T

http://identifiers.org/hco/1/GRCh38#85177147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145713692-A-C

85177283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713549-T-C

85177653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713287-T-C

85177699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713248-G-C

85177997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713035-G-A

85177997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145713035-G-T

85178077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712959-A-G

http://identifiers.org/hco/1/GRCh38#85178103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145712933-A-C

85178103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712933-A-G

85178103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712933-A-T

85178109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712927-T-C

85178190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, missense_variant
orthologous variants: 145712851-A-G

85178190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, missense_variant
orthologous variants: 145712851-A-T

85178235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, missense_variant
orthologous variants: 145712806-A-G

85178252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 145712789-T-C

85178259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, missense_variant
orthologous variants: 145712782-T-C

http://identifiers.org/hco/1/GRCh38#85178292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145712753-C-A

85178292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712753-C-T

85178364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712686-G-C

85178364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712686-G-T

85178433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712629-T-C

85179142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712146-C-G

85179164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145712122-A-G

85179295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145711983-A-G

85179337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145711941-T-G

85179371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145711912-T-C

85179814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145711233-T-C

85179932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145711126-T-C

85180776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: 145709285-A-G

http://identifiers.org/hco/1/GRCh38#85181016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145709046-C-A

85181772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708504-T-C

http://identifiers.org/hco/1/GRCh38#85181793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145708486-C-A

85181793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708486-C-T

85181796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708483-T-C

85181851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708432-A-G

85181851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708432-A-T

85181882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708407-A-G

85181958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708322-A-G

85181958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708322-A-T

85182067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708192-G-A

85182067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 145708192-G-T

http://identifiers.org/hco/1/GRCh38#85182102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145708162-C-A

85182102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145708162-C-G

85182126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145708138-A-T

85182162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145708102-A-G

http://identifiers.org/hco/1/GRCh38#85182231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145708033-C-A

85182231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145708033-C-G

85182324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707940-G-C

85182348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707916-A-G

85182423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707841-T-C

85182426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707838-G-C

85182526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707738-T-C

85182559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707705-G-A

85182559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707705-G-T

85182615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707649-T-C

http://identifiers.org/hco/1/GRCh38#85182635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145707629-A-C

85182635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 145707629-A-T

http://identifiers.org/hco/1/GRCh38#85182662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145707602-A-C

85182818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 145707446-G-A

85183167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145707109-T-A

http://identifiers.org/hco/1/GRCh38#85183217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145707059-A-C

85183242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145707037-T-C

85183286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145706999-G-C

85183286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145706999-G-T

85183389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145706202-T-C

85183616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145705989-T-C

85184150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145705131-G-T

85190192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704728-G-A

85190192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 145704728-G-T

85190244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 145704697-A-G

85190335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704615-C-T

85190380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704570-T-C

85190437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704513-C-T

85190455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704495-G-A

85190518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704450-G-A

85190520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 145704448-T-C

85190578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704390-T-C

85190728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704243-G-A

85190728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145704243-G-C

85190766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145704209-A-G

85190784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145704191-T-A

85190950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145703901-G-A

85191014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145703837-T-G

85191016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145703835-T-C

85191156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145703713-T-C

85192125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145703113-A-T

85193174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145701557-A-T

85193195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145701536-G-C

http://identifiers.org/hco/1/GRCh38#85193274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145701458-C-A

85193435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145701324-T-G

85193535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145701216-C-T

85194733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700605-C-G

85194733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700605-C-T

85194997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700208-A-G

http://identifiers.org/hco/1/GRCh38#85195001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145700204-A-C

85195002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700203-T-C

85195005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700200-A-G

http://identifiers.org/hco/1/GRCh38#85195032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145700172-C-A

85195032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700172-C-T

85195040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700164-G-A

85195116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700104-C-T

85195137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145700079-G-A

85195326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699992-C-T

85195438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699953-C-G

85195548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699879-T-A

85195680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699744-C-T

85195731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699701-A-G

85195755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699678-A-G

http://identifiers.org/hco/1/GRCh38#85195808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145699627-C-A

85195860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699600-A-G

http://identifiers.org/hco/1/GRCh38#85195861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145699599-A-C

85195895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699572-T-C

85196120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699242-T-C

85196175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699178-T-A

85196201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699151-A-G

85196325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145699025-A-T

85196479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145698860-G-A

85196499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145698834-T-C

85197412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 145697454-T-C

85198763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145696540-A-G

85199659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695673-T-C

85199659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695673-T-G

85199670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695662-T-C

85199769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695602-G-A

85199856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695518-A-G

85199991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695368-C-T

85200003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145695356-G-C

85200208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145694971-A-G

85200218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145694960-G-A

85200218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 145694960-G-C

85200344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 145694830-C-T

85200523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous variant
orthologous variants: 145694654-G-A

http://identifiers.org/hco/1/GRCh38#85200533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145694644-C-A

85200533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694644-C-G

85200560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694617-C-T

85200644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694533-T-A

85200644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694533-T-C

http://identifiers.org/hco/1/GRCh38#85200758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#145694419-C-A

85200758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694419-C-T

85200872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145694317-G-A

85200889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous_variant, undefined
orthologous variants: 145694300-G-A

85200889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous_variant, undefined
orthologous variants: 145694300-G-T

85200919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous_variant, undefined
orthologous variants: 145694264-G-A

85200919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous_variant, undefined
orthologous variants: 145694264-G-C

85200919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous_variant, undefined
orthologous variants: 145694264-G-T

85200983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145694224-G-A

85200983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145694224-G-C

85200983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145694224-G-T

85201224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145694013-C-T

85201313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense variant
orthologous variants: 145693936-G-A

85201345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: synonymous variant
orthologous variants: 145693906-T-C

85201413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145693857-G-T

85201568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: missense_variant, undefined
orthologous variants: 145693771-C-T

http://identifiers.org/hco/1/GRCh38#85201588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#145693751-C-A

85201626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 5 prime UTR variant
orthologous variants: 145693712-G-A

85201626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25841
most severe consequence: 5 prime UTR variant
orthologous variants: 145693712-G-T