82629702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100366999-T-C

82631156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100368122-A-G

http://identifiers.org/hco/4/GRCh38#82631236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100368199-C-A

82631236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100368199-C-G

82631236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100368199-C-T

82631254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100368216-A-G

http://identifiers.org/hco/4/GRCh38#82631305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100368284-A-C

82631305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3 prime UTR variant
orthologous variants: 100368284-A-G

82631406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100368378-C-T

82631417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100368389-C-T

82631420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100368392-G-A

82631469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100368441-G-A

82631469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100368441-G-T

http://identifiers.org/hco/4/GRCh38#82631488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100368460-A-C

82631488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100368460-A-G

http://identifiers.org/hco/4/GRCh38#82631531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100368503-C-A

82631531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100368503-C-T

82631564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100368537-G-T

82631569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100368542-G-A

82631569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100368542-G-C

http://identifiers.org/hco/4/GRCh38#82631628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100369174-C-A

http://identifiers.org/hco/4/GRCh38#82631660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100369205-C-A

82631660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100369205-C-G

82631924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100369476-T-G

http://identifiers.org/hco/4/GRCh38#82631979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100369554-A-C

http://identifiers.org/hco/4/GRCh38#82632018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100369603-C-A

82632018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100369603-C-T

82632069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100369652-G-A

82632069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100369652-G-C

82634866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100372554-G-C

82635149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100372811-G-A

82635778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100373145-C-T

http://identifiers.org/hco/4/GRCh38#82636167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100373522-A-C

82636176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100373531-G-A

http://identifiers.org/hco/4/GRCh38#82636539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100373612-A-C

82636591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 100373662-C-T

82636607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100373678-G-A

82636610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100373681-G-A

82636659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100373729-T-A

82636727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100373797-C-G

82636729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100373799-A-G

82636730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100373800-G-A

82636730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100373800-G-T

http://identifiers.org/hco/4/GRCh38#82640160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100374202-C-A

http://identifiers.org/hco/4/GRCh38#82640286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100374350-C-A

82640319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100374429-A-T

82640377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100374518-C-T

http://identifiers.org/hco/4/GRCh38#82640418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100374609-A-C

82640664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100374835-G-A

82640788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100374962-G-C

82640793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100374967-G-C

82641489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100375455-G-T

http://identifiers.org/hco/4/GRCh38#82641516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100375482-A-C

82641516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100375482-A-G

82641674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100375605-T-C

82641693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100375623-G-A

82641948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100375878-C-T

82644494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378253-A-G

82644499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378258-C-T

82644669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378435-G-A

http://identifiers.org/hco/4/GRCh38#82644680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100378446-C-A

http://identifiers.org/hco/4/GRCh38#82644869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100378623-C-A

82644912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378665-C-T

http://identifiers.org/hco/4/GRCh38#82645368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100378796-A-C

82645368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378796-A-T

82645504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100378928-G-T

82645734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100379291-A-G

http://identifiers.org/hco/4/GRCh38#82645916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100379485-A-C

82645916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100379485-A-G

82646039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100379595-T-C

82646283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100379821-C-T

82647203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100381153-A-T

82647602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100381486-G-A

82647678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100381523-C-T

http://identifiers.org/hco/4/GRCh38#82653178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100386632-C-A

82653193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100386647-T-C

82653330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100386750-A-G

82653584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100386995-T-C

http://identifiers.org/hco/4/GRCh38#82653673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100387064-C-A

82653711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387138-G-A

82653711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387138-G-T

82654190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387678-A-G

82654214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387702-C-T

82654244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387728-G-C

82654244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387728-G-T

82654439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100387870-G-C

82654840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100388237-G-A

82654874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100388275-G-A

82655225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100389769-T-C

82655327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100389869-A-G

82655370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100389905-T-C

82655486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100390000-G-A

82655703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100390198-T-C

82655889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100390310-T-C

82655908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100390329-G-T

82660478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391414-T-A

82660478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391414-T-G

82660492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391428-T-A

http://identifiers.org/hco/4/GRCh38#82660495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100391431-C-A

82660570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391504-T-A

82660620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391550-C-G

82660652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391584-C-T

82660675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391609-T-C

82660684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391618-A-G

http://identifiers.org/hco/4/GRCh38#82660688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100391620-C-A

82660688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391620-C-T

82660735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391666-T-C

82660789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391726-G-A

82660789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391726-G-T

82660870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 100391808-T-C

82660917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100391855-A-G

82660940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: 100391877-C-T

82660961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: 100391896-A-G

82660961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, stop_gained
orthologous variants: 100391896-A-T

82660971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 100391906-A-G

82660971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: 100391906-A-T

82660980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: 100391915-G-A

82660980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: 100391915-G-T

http://identifiers.org/hco/4/GRCh38#82661008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100391930-C-A

82661040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, stop_gained
orthologous variants: 100391965-G-A

82661098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392255-T-C

82661099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392256-G-A

http://identifiers.org/hco/4/GRCh38#82661184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100392337-C-A

82661184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392337-C-T

http://identifiers.org/hco/4/GRCh38#82661205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100392358-C-A

82661314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392543-G-A

82661478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392698-T-C

82661603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100392817-A-G

http://identifiers.org/hco/4/GRCh38#82667044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100394253-C-A

82667127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100394340-C-T

82667288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395070-G-A

82667292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395074-G-A

82667417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395202-C-G

82667492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395269-T-C

82667805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395542-G-C

82667827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100395552-G-A

http://identifiers.org/hco/4/GRCh38#82668558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100396166-A-C

http://identifiers.org/hco/4/GRCh38#82669025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100396594-C-A

82669154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100396716-T-C

82669194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100396759-A-G

82669265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100396824-G-A

82669275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100396834-T-G

82669512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100396981-T-C

82675934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100401963-T-C

82676019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402048-T-C

82676098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402106-C-G

82676144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402149-G-A

82676374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402510-G-A

82676390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402526-G-A

82676421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402556-T-C

http://identifiers.org/hco/4/GRCh38#82676645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100402710-C-A

82676645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402710-C-T

82676704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402751-C-G

82677020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100402992-C-T

82677084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403065-A-G

82677554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403515-G-A

82677777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403718-T-C

82677805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403756-C-T

82677863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403815-G-A

82677863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403815-G-T

82677994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100403938-C-G

82678340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404250-G-A

82678442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404336-C-T

82678656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404546-A-G

82678772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404669-T-C

82678802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404701-T-C

82679293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404952-A-T

82679295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404954-A-G

82679295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404954-A-T

82679296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404955-G-A

82679296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404955-G-C

82679296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100404955-G-T

82679374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405008-G-A

82679437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405038-G-A

82679529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405137-C-G

82679640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405237-T-C

82679688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405274-C-T

82680057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405648-C-T

82680074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405665-C-T

82680084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100405675-G-A

82680382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406173-C-T

82680409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406200-G-C

82680588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406349-G-A

82680588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406349-G-T

82680599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406360-A-G

82680599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406360-A-T

82680611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406365-T-G

82680612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406366-G-A

82680612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406366-G-T

82680633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406387-T-C

82680633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406387-T-G

82680637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406391-T-C

82680727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100406465-A-G

82680748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100406493-G-A

http://identifiers.org/hco/4/GRCh38#82680791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100406535-C-A

82680791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100406535-C-T

82680830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100406574-C-T

http://identifiers.org/hco/4/GRCh38#82680888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100406632-C-A

82680888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense variant
orthologous variants: 100406632-C-T

82680941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406686-G-C

82680941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406686-G-T

82680970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406709-T-A

82680970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406709-T-G

82681060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406797-G-T

82681080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100406820-G-A

82683578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407077-G-A

82684098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407253-C-G

82684098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407253-C-T

82684116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407273-G-A

82684127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407284-G-C

82684319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407449-G-A

82684389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407456-A-T

82684626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407758-G-A

82684675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100407912-T-C

82685009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100408505-C-G

http://identifiers.org/hco/4/GRCh38#82685240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100408719-C-A

82685241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100408720-C-T

82685259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100408737-T-G

82685381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100408880-T-C

82685630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409071-C-G

82685699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409125-A-G

82685704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409130-T-C

82685840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409319-G-A

82685843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409322-T-C

82685925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409415-C-T

82685932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409422-C-T

82685981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100409471-C-T

82686692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100410003-G-A

82686692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100410003-G-C

82687579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100414244-C-T

http://identifiers.org/hco/4/GRCh38#82687590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100414259-C-A

82687662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100414308-T-G

82687901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100414541-A-T

82688075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100414794-A-G

82688389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100415056-G-A

http://identifiers.org/hco/4/GRCh38#82688526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100415178-C-A

82689176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100417828-G-A

82689229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100417878-C-T

82689870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100418492-C-T

82690462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100419027-C-T

82690560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100419081-T-A

82690563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100419084-C-T

82690691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100419213-T-G

82690916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100419427-A-G

82695945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100421916-T-G

82695973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100421945-G-A

82695973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100421945-G-T

82696195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100422165-T-C

82696268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100422237-T-C

82696798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100422765-G-A

82696894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100422856-A-G

82697005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100422966-C-G

82697593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427590-A-G

82697657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427658-G-A

82697755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427736-T-C

82697815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427768-G-A

82697937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427848-T-C

82698059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100427955-G-T

82698167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100428011-G-C

82698205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100428049-T-C

http://identifiers.org/hco/4/GRCh38#82698245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100428075-C-A

82698374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100428095-G-A

82698450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100428165-G-T

http://identifiers.org/hco/4/GRCh38#82698549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100428251-C-A

82698549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100428251-C-T

82702780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100440214-G-T

http://identifiers.org/hco/4/GRCh38#82702921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100440315-C-A

82702925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100440318-G-A

82703081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100440711-T-A

82703081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100440711-T-C

82703205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100440831-G-T

82703702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100441359-T-G

82703808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100441465-T-G

82703813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100441470-C-T

82704465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100442096-T-C

82704490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100442120-T-C

82704622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100442258-T-C

http://identifiers.org/hco/4/GRCh38#82704855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100442488-C-A

82704902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100442925-A-G

82705052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443027-T-G

82705217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443192-T-A

82705283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 100443243-C-T

82705373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100443333-A-G

82705373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100443333-A-T

http://identifiers.org/hco/4/GRCh38#82705379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100443339-C-A

82705379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100443339-C-G

82705379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: synonymous variant
orthologous variants: 100443339-C-T

82705517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443473-G-A

82705517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443473-G-T

82705554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443517-G-A

82705554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443517-G-T

82705576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100443538-T-C

82705938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100445123-G-A

http://identifiers.org/hco/4/GRCh38#82705947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100445132-A-C

http://identifiers.org/hco/4/GRCh38#82705991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100445176-A-C

82706179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100445362-C-T

82706333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100445491-G-A

http://identifiers.org/hco/4/GRCh38#82706585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100445727-A-C

82706829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100445927-T-C

http://identifiers.org/hco/4/GRCh38#82708536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100448353-C-A

82708608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448423-T-A

82708681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448496-T-C

82708712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448525-A-T

82708744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448549-T-A

82708744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448549-T-C

82708836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448631-C-T

82709123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100448902-C-T

82710087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100451216-G-A

http://identifiers.org/hco/4/GRCh38#82710224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100451268-C-A

82710330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100451391-T-C

82710330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100451391-T-G

82710579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100451610-G-A

82710916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452127-T-C

82710916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452127-T-G

82711061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452251-G-A

82711061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452251-G-C

82711064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452254-T-A

82711064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452254-T-C

http://identifiers.org/hco/4/GRCh38#82711092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100452281-C-A

82711094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452283-T-A

82711094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452283-T-G

http://identifiers.org/hco/4/GRCh38#82711188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100452361-C-A

82711188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452361-C-G

82711188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100452361-C-T

82712905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100454434-G-A

82712982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100454513-G-C

82713034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100454564-G-A

82713034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100454564-G-T

82713088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100454604-G-A

82717144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100457421-T-C

82717241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100457510-T-G

82717407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100457660-C-T

82717482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100457733-A-G

82724631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100460119-T-C

82724974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100460806-G-A

82725157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100461047-G-A

82725376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100461219-A-G

82725478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100461289-T-C

82725478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100461289-T-G

82731001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100463430-G-A

82731228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100463636-A-T

82731673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100463972-C-T

http://identifiers.org/hco/4/GRCh38#82731963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100464174-C-A

82732448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464452-G-T

82732833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464654-G-C

82732884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464691-C-T

82732920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464727-T-C

82733124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464876-T-G

82733153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100464882-G-A

82733775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100465381-C-G

82733776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100465382-C-T

http://identifiers.org/hco/4/GRCh38#82734022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100465585-C-A

82734081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100465623-T-C

82734458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100465987-C-T

82734482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100466009-T-C

82734639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100466543-A-G

82734673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100466577-G-C

82734675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100466579-C-T

82737062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467477-C-T

82737072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467487-A-G

82737098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467513-C-T

82737099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467514-G-A

82737099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467514-G-T

82737148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467564-T-C

82737338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467749-C-T

82737352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467763-T-A

82737352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467763-T-C

82737543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100467939-A-G

82737683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468088-G-T

82737878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468259-A-G

82737937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468319-T-C

82737999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468367-G-T

82738041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468419-G-A

82738196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468688-G-A

82738200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468692-C-G

82738229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468719-C-G

82738295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468770-G-A

http://identifiers.org/hco/4/GRCh38#82738304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100468779-C-A

82738355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100468827-G-C

82738475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469059-T-A

82738475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469059-T-G

http://identifiers.org/hco/4/GRCh38#82738635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100469303-C-A

82738810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469473-T-A

82738823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469486-C-T

82738981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469590-G-A

82739007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469616-T-C

82739104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469715-T-C

82739163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469759-C-T

82739250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100469868-A-G

82739357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100469979-C-T

82739381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron_variant, undefined
orthologous variants: 100470003-G-A

82739527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470146-C-G

82739527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470146-C-T

82739541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470161-C-T

82739670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470243-C-T

82741417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470627-G-A

82741417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470627-G-T

82741546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470740-A-G

82741596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470788-C-G

82741650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470842-A-G

http://identifiers.org/hco/4/GRCh38#82741669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100470862-A-C

82741678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470871-G-A

82741687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470876-C-T

82741700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100470889-A-G

82741909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471029-A-G

82742159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471130-T-C

82742195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471167-C-T

82742218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471189-G-A

82742273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471229-G-A

82746075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471852-T-A

82746177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471955-G-A

82746209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100471986-T-C

82746269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100472043-G-A

82746690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100472516-A-G

82746709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100472535-G-C

82747346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473123-G-A

82747346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473123-G-C

82747413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473190-T-C

82747451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473226-C-T

82747584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473354-G-A

82747872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473610-A-G

82747906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473628-G-T

82748002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473722-T-C

82748153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473848-G-T

82748202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473900-C-T

http://identifiers.org/hco/4/GRCh38#82748246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100473940-C-A

82748275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100473970-G-A

82748305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100474001-C-T

82748381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100474070-C-G

82748385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100474074-G-A

82748398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100474087-C-T

http://identifiers.org/hco/4/GRCh38#82752387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100475988-A-C

82752412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476012-A-G

82752613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476210-C-G

http://identifiers.org/hco/4/GRCh38#82753239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100476386-C-A

82753261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476413-T-C

82753261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476413-T-G

82753312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476464-G-A

82753312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476464-G-T

82753321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476473-G-A

82753321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476473-G-T

82753462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476606-C-T

82753463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476607-G-A

82753478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476622-C-G

82753478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476622-C-T

82753555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476699-A-G

82753561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476705-G-A

82753660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476780-T-C

82753696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476799-T-C

82753863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100476936-C-T

82754159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100477227-G-T

82754354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478484-G-A

82754363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478495-C-T

http://identifiers.org/hco/4/GRCh38#82754522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100478622-A-C

82754522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478622-A-G

82754526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478626-T-A

82754526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478626-T-C

82754551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478650-T-A

82755754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478904-C-G

82755796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100478946-T-C

82755990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100479157-T-C

82756063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100479219-C-G

82760881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481117-C-T

82760916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481145-A-G

82761056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481279-A-G

82761108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481331-A-G

82761360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481563-C-T

82761373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481577-G-A

82761383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100481587-T-C

82768834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100482973-G-T

82769259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100483994-T-A

82769306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100484042-A-G

82769371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100484105-C-T

http://identifiers.org/hco/4/GRCh38#82769395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100484128-C-A

82769500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100484228-G-A

82778826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100486683-A-G

82779573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488460-C-T

82779586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488473-A-T

82779655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488526-C-T

82779666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488537-G-A

82779666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488537-G-T

82779699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488570-C-T

82779717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488590-T-C

82779881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488740-T-C

http://identifiers.org/hco/4/GRCh38#82779995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100488851-C-A

82780123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488963-A-T

82780153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488994-T-C

82780153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100488994-T-G

82780162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489003-T-C

82780310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489155-C-T

82780378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489216-T-C

82780385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489222-C-T

82780402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489239-G-C

82780500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489734-C-T

82780680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100489908-C-T

82780874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100490035-G-C

82780889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100490047-A-G

82780893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100490051-C-T

82780921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100490080-T-C

82780986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100490126-G-A

82787112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491574-A-G

82787115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491577-G-A

82787141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491603-C-G

82787141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491603-C-T

82787189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491639-A-T

82787261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491712-C-T

82787307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100491753-C-T

82789349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100494154-T-G

82791454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100496101-C-G

82791454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100496101-C-T

82791523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100496174-G-A

82793216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497454-G-A

82793288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497526-G-T

82793295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497533-G-A

82793295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497533-G-T

82793298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497536-G-A

82793432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497668-G-T

82793452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100497686-T-C

82794307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100498654-C-T

82794313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100498659-C-T

http://identifiers.org/hco/4/GRCh38#82794326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100499582-A-C

82794461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100499741-G-A

82794602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100499852-A-T

82794640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100499894-C-T

82794669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100499915-A-G

82794669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100499915-A-T

http://identifiers.org/hco/4/GRCh38#82795151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100500277-A-C

82795196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100500329-C-T

82795246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100500379-G-C

82795246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100500379-G-T

82795883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100500650-T-A

82796371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100500851-C-G

82796530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501011-G-A

82796681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501165-A-G

82796699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501183-G-A

82796835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501324-T-C

82796874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501369-A-G

82796937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501428-C-T

82797047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501523-C-G

82797047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501523-C-T

82797444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100501786-G-A

82798156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502639-G-T

82798195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502665-A-G

82798198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502668-G-A

82798198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502668-G-C

82798198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502668-G-T

http://identifiers.org/hco/4/GRCh38#82798248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100502708-C-A

82798248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: intron variant
orthologous variants: 100502708-C-G

82798336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense_variant, undefined
orthologous variants: 100502792-G-A

82798363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense_variant, undefined
orthologous variants: 100502819-C-T

http://identifiers.org/hco/4/GRCh38#82798419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100502875-C-A

82798512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: missense_variant, undefined
orthologous variants: 100502953-C-T

82798629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503007-T-C

82798630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503008-T-C

82798630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503008-T-G

82798668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503038-A-T

82798682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503047-G-A

82798682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503047-G-T

http://identifiers.org/hco/4/GRCh38#82798710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#100503056-C-A

82798710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503056-C-T

82798718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503064-A-G

82798718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503064-A-T

82798726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503072-A-G

82798726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503072-A-T

82798727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100503073-G-T

http://identifiers.org/hco/4/GRCh38#82798764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#100503110-C-A

82798764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503110-C-T

82798779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503125-G-A

82798779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21088
most severe consequence: 5 prime UTR variant
orthologous variants: 100503125-G-T