68731932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808358-G-A

68732083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808491-C-G

68732083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808491-C-T

http://identifiers.org/hco/3/GRCh38#68732225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96808616-C-A

68732225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808616-C-G

68732225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808616-C-T

68732269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808659-G-A

68732412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808804-T-C

68732412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808804-T-G

http://identifiers.org/hco/3/GRCh38#68732563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96808970-C-A

68732563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96808970-C-T

68732762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96809145-A-G

68732993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3 prime UTR variant
orthologous variants: 96809376-G-T

68733075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809458-G-A

68733075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809458-G-T

68733104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 96809487-T-C

http://identifiers.org/hco/3/GRCh38#68733109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96809492-C-A

68733109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809492-C-G

68733109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809492-C-T

68733114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809496-C-G

68733114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809496-C-T

68733118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96809500-G-T

68733156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 96809536-A-G

http://identifiers.org/hco/3/GRCh38#68733285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96809659-A-C

68733285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96809659-A-G

68733377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96809757-A-T

68733455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96809841-G-A

68733455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96809841-G-C

http://identifiers.org/hco/3/GRCh38#68733516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96809902-A-C

68733516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96809902-A-T

68734045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810285-G-A

68734193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810424-T-G

68734204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810435-A-G

68734395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810800-C-T

68734396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810801-G-A

68734396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96810801-G-C

http://identifiers.org/hco/3/GRCh38#68734493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96810959-A-C

68735131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96811624-C-G

68735131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96811624-C-T

68735398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96812242-A-T

68735605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96816771-A-G

http://identifiers.org/hco/3/GRCh38#68735998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96817540-C-A

68736417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96817930-C-G

68736760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96818285-G-A

68736760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96818285-G-T

68736787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96818312-G-A

68737401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96818970-A-G

68737438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96819007-C-G

68737785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96819437-A-G

68737864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96819580-G-T

68738192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96819909-A-G

68738262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96819975-C-T

68738371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820058-G-A

68738397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820085-T-C

http://identifiers.org/hco/3/GRCh38#68738399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96820087-A-C

68738443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820127-G-A

68738842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820485-T-C

68738907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820533-T-A

68738947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820573-A-G

http://identifiers.org/hco/3/GRCh38#68738960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96820586-C-A

68738974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820600-T-G

68738998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820627-T-C

68738998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820627-T-G

68739048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820685-T-A

68739048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820685-T-C

68739243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820880-C-T

http://identifiers.org/hco/3/GRCh38#68739266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96820901-C-A

68739280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820915-G-C

68739280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96820915-G-T

68742009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825115-T-C

68742105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825208-G-T

68742230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825332-C-T

68742237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825339-G-A

68742339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825481-A-G

68742347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825489-A-T

68742375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825517-T-A

http://identifiers.org/hco/3/GRCh38#68742649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96825719-C-A

68743016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825962-C-G

68743016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96825962-C-T

http://identifiers.org/hco/3/GRCh38#68743104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96826022-A-C

68743273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96826185-A-T

68745079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96829767-A-G

68745094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96829781-C-T

68745124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96829809-T-C

68745276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96829954-T-C

http://identifiers.org/hco/3/GRCh38#68745434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96830109-A-C

68745434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96830109-A-G

68745552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96830225-G-A

68745552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96830225-G-C

68745552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96830225-G-T

68745629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96830297-G-A

68746715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832225-G-A

68746725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832234-C-G

http://identifiers.org/hco/3/GRCh38#68746761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96832272-A-C

68746790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832306-T-G

http://identifiers.org/hco/3/GRCh38#68746970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96832486-C-A

68746981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832497-C-T

68747005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832510-G-A

http://identifiers.org/hco/3/GRCh38#68747691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96832783-A-C

68747691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832783-A-G

68747709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96832801-A-G

68747948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96833002-C-T

68747998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96833042-T-C

68749504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96834237-T-C

68749593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96834315-T-C

68749879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96834576-G-A

68750620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96835063-A-G

68751172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96835630-T-C

68751208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96835659-C-T

http://identifiers.org/hco/3/GRCh38#68751302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96835743-A-C

68751347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96835790-C-T

http://identifiers.org/hco/3/GRCh38#68751751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96839196-C-A

68751751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839196-C-T

68751782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839226-T-G

68751869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839285-C-T

68752170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839570-G-A

68752210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839607-A-G

68752258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839655-G-A

68752289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839680-C-T

68752309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96839700-C-T

68752650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840549-T-A

68752700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840590-C-T

68752819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840677-T-C

68752819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840677-T-G

68752846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840704-G-A

68752846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840704-G-C

68752969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: synonymous variant
orthologous variants: 96840827-C-T

68752993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: synonymous variant
orthologous variants: 96840851-G-T

68753017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 96840875-A-T

68753027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840885-T-C

68753043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840900-C-G

http://identifiers.org/hco/3/GRCh38#68753102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96840962-C-A

68753111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840973-A-G

http://identifiers.org/hco/3/GRCh38#68753112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96840974-C-A

68753120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840999-G-A

68753120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96840999-G-T

68753382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841160-T-C

68753555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841214-C-T

68753726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841255-A-T

68754011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841531-G-T

68754044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841566-T-C

68754152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841643-T-C

68754267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841735-C-T

68754311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96841771-C-T

68754561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96842079-C-G

68754604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96842111-A-G

68755103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96842566-T-G

68755174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96842648-C-T

68757373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843046-T-C

68757455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843133-C-T

http://identifiers.org/hco/3/GRCh38#68757838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96843516-C-A

68757937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843605-T-C

68757991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843659-T-A

68757991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843659-T-C

68758189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96843816-T-G

68759083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844142-A-G

68759327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844353-C-T

http://identifiers.org/hco/3/GRCh38#68759345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96844371-C-A

68759429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844456-G-T

http://identifiers.org/hco/3/GRCh38#68759554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96844563-A-C

68759554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844563-A-T

68759748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844735-G-C

68759892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96844878-T-C

68760077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845072-A-G

68760379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845382-T-G

http://identifiers.org/hco/3/GRCh38#68760403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96845403-A-C

68760450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845445-C-T

68760735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845707-T-C

68760839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845811-C-T

68760939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96845899-A-G

http://identifiers.org/hco/3/GRCh38#68761373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96846317-A-C

68761373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96846317-A-G

http://identifiers.org/hco/3/GRCh38#68762196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96847222-C-A

http://identifiers.org/hco/3/GRCh38#68762304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96847438-C-A

68762304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96847438-C-G

68762323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96847457-A-T

68763227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96847984-G-C

68763349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848101-T-A

68763440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848185-G-A

68763573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848300-A-G

http://identifiers.org/hco/3/GRCh38#68763697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96848422-C-A

68763697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848422-C-G

68763749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848471-T-C

68763788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848510-A-G

68764241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96848854-A-T

68764594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96849230-G-C

68765247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96867332-T-C

68765287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96867372-T-C

68765541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96867690-C-G

68765856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96868007-C-T

68765878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96868029-A-G

68765879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96868030-G-A

68765880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96868031-G-T

68767704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96869214-T-C

68767721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96869232-C-G

68786551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885288-T-C

68786633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885374-T-C

68786679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885421-T-C

68786716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885446-G-C

68786721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885451-T-C

68786993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885751-G-T

68787116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885877-G-T

68787193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96885954-G-A

68787389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886152-T-C

68787541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886303-A-G

68787677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886434-T-C

68787703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886463-C-G

68787824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886579-G-A

68787843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886610-A-G

68787895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96886666-T-C

68790048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96887551-G-C

http://identifiers.org/hco/3/GRCh38#68790145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96887647-A-C

68790145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96887647-A-G

68790703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888453-G-T

68790730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888483-A-T

68790734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888487-G-A

http://identifiers.org/hco/3/GRCh38#68790748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96888501-A-C

68790766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888524-G-A

68791021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888770-G-A

68791120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888833-G-A

68791125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96888838-C-G

http://identifiers.org/hco/3/GRCh38#68791281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96888952-A-C

http://identifiers.org/hco/3/GRCh38#68791352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96889018-A-C

68791383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96889049-A-G

68791956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891287-T-C

68792309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891662-T-C

68792410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891761-T-C

68792458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891808-G-T

68792493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891843-A-G

68792543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96891893-G-C

68792666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96892012-C-T

68792901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96892257-A-G

68793166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96892519-T-C

http://identifiers.org/hco/3/GRCh38#68793843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96893301-A-C

68793843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893301-A-T

68794048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893510-T-C

68794053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893515-C-G

68794110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893574-T-C

68794227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893687-C-T

http://identifiers.org/hco/3/GRCh38#68794288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96893744-A-C

68794288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893744-A-T

68794360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96893799-A-G

68795066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96896540-A-G

68795159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96896597-G-A

68795159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96896597-G-C

68796169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96897533-C-T

68796174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96897538-G-A

68796410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96897819-C-T

68796502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96897959-G-T

http://identifiers.org/hco/3/GRCh38#68800376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96908731-A-C

68800419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96908759-C-G

http://identifiers.org/hco/3/GRCh38#68800474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96908810-A-C

68800525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96908857-T-C

68800546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96908878-A-G

68800701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96909047-G-A

68800994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96909312-G-T

68801003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96909321-G-T

68801981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96914943-C-T

68802025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96914989-G-A

68802026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96914990-T-A

http://identifiers.org/hco/3/GRCh38#68802438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96916043-C-A

68802438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916043-C-T

68802445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916050-G-A

68802581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916195-C-T

http://identifiers.org/hco/3/GRCh38#68802656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96916269-C-A

68802696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916309-A-G

68802807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916419-G-T

68803082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916693-G-A

68803112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96916761-G-A

http://identifiers.org/hco/3/GRCh38#68803492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96917832-C-A

68803520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96917860-C-T

68803543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96917883-A-G

68803672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96918063-A-T

68803730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96918109-G-A

http://identifiers.org/hco/3/GRCh38#68803783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96918170-C-A

68803783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96918170-C-T

68806080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96918441-G-A

68806306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96918640-T-G

68807067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96920914-C-T

68807127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96920964-A-T

68807198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96921055-A-G

68807698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96921548-G-A

68807698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96921548-G-C

68808521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96922252-A-G

68808606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96922338-T-G

http://identifiers.org/hco/3/GRCh38#68808779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96922488-A-C

68808856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96922563-G-C

68820211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96925436-G-A

68820211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96925436-G-T

68820986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96926127-G-C

68821232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96926350-C-G

68821938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96926731-G-A

68821992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96926779-C-G

68822267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96927045-C-T

68822409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96927160-T-C

68822412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96927163-G-A

68834004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96933442-A-G

68834253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96934538-C-G

68834318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96934612-G-C

68834324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96934618-G-A

68834358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96934658-A-T

68834617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96934902-T-A

68834979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935240-C-G

68835147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935357-A-G

68835222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935388-C-G

68835600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935711-G-C

68835600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935711-G-T

http://identifiers.org/hco/3/GRCh38#68835762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96935869-C-A

68835762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935869-C-T

68835770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96935870-G-C

68836328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96936380-G-A

68836472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96936510-C-G

68836540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96936603-A-G

68836576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96936664-T-C

http://identifiers.org/hco/3/GRCh38#68838339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96956876-A-C

68838360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96956897-T-C

68838471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96957340-T-C

68838475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96957344-G-A

68838576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96957432-G-A

68838738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96957833-T-A

68838738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96957833-T-C

http://identifiers.org/hco/3/GRCh38#68838754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96957849-C-A

http://identifiers.org/hco/3/GRCh38#68838850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96957950-A-C

68839362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96958485-T-C

68839362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96958485-T-G

68839511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96958617-G-A

68839511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96958617-G-T

68839729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96958831-A-G

68839907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96959008-G-C

68839940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96959040-C-G

68847753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960443-G-C

68847771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960461-A-G

68847775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960465-G-A

68847787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960477-G-C

68847803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960493-G-A

68847812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960502-C-T

68847826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960516-G-A

http://identifiers.org/hco/3/GRCh38#68847827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96960517-C-A

68847839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960529-T-A

68847974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96960655-C-T

68848369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961030-T-C

68848424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961088-C-T

68848573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961215-G-A

68848597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961237-A-G

68848771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961521-C-T

68848792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961542-C-G

68848792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961542-C-T

68848801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961551-C-T

http://identifiers.org/hco/3/GRCh38#68848932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96961683-C-A

68849005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961743-T-C

68849028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961766-T-C

68849083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96961825-T-C

68849318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96962056-T-G

68852659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96962381-G-A

68852659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96962381-G-C

http://identifiers.org/hco/3/GRCh38#68852904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96963075-C-A

68853006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963178-C-G

68853044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963215-G-C

68853113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963286-T-C

68853166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963340-G-C

68853182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963356-A-G

68853210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963384-T-C

68853422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963595-A-G

68853478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963649-C-G

68853584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963756-A-G

68853606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96963778-A-G

68853660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96964344-A-G

68853748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96964431-G-A

68853773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96964455-C-G

68853805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96964487-G-A

http://identifiers.org/hco/3/GRCh38#68853833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96964634-A-C

68854142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96964922-A-G

http://identifiers.org/hco/3/GRCh38#68854222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96964995-A-C

68854237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965011-G-A

68854330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965095-C-G

68854554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965308-T-A

68854630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965388-T-C

68854858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965582-G-A

68854858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965582-G-C

68854876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965601-C-G

68854911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965636-C-T

http://identifiers.org/hco/3/GRCh38#68854981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96965707-C-A

68854981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965707-C-G

http://identifiers.org/hco/3/GRCh38#68855068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96965794-A-C

http://identifiers.org/hco/3/GRCh38#68855070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96965796-A-C

http://identifiers.org/hco/3/GRCh38#68855176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96965882-A-C

68855176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96965882-A-G

http://identifiers.org/hco/3/GRCh38#68855225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96965933-C-A

68855289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966001-C-T

68855290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966002-C-G

68855386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966131-T-A

68855455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966200-T-A

68855472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966214-G-A

68855511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966255-C-T

68855644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966827-T-C

68855681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966864-T-C

68855742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966925-C-T

68855762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96966945-C-T

http://identifiers.org/hco/3/GRCh38#68855952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96967124-C-A

68856235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967369-G-A

68856447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967668-C-T

68856455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967687-C-T

68856475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967707-A-G

68856493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967935-T-C

68856495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96967937-C-T

68856825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968277-G-A

http://identifiers.org/hco/3/GRCh38#68856960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96968415-A-C

68857021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968473-T-A

68857102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968550-T-C

68857140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968596-G-A

68857140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968596-G-T

68857238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968692-C-G

68857238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968692-C-T

68857519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968956-T-C

68857548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96968986-T-A

68857919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969247-G-A

68858091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969376-G-A

68858091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969376-G-T

68858200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969440-G-A

68858208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969448-G-T

http://identifiers.org/hco/3/GRCh38#68858216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96969456-A-C

68858407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969613-G-C

68858407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969613-G-T

68858436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969646-G-A

68858454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969664-G-A

68858455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96969665-A-G

68859203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96971671-G-A

68859359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96971818-G-T

68859672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96972131-A-T

68859686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96972145-G-A

68859742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96972212-C-T

68859813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96972282-T-A

68873144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96976159-A-G

http://identifiers.org/hco/3/GRCh38#68873198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96976210-A-C

http://identifiers.org/hco/3/GRCh38#68873305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96976277-A-C

68873310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96976282-C-G

68873329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96976292-C-T

68873333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96976296-G-C

68873502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977135-G-A

68873502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977135-G-T

68873578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977210-C-T

http://identifiers.org/hco/3/GRCh38#68873588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96977220-C-A

68873590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977222-A-G

68873675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977304-C-G

68873675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977304-C-T

68873692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977321-A-G

68873739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977367-C-T

68874085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977691-G-C

68874105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977713-C-G

68874138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96977746-T-C

68874482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96978089-C-T

68874542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96978149-G-C

68874732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96978331-C-T

68875157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979046-G-C

68875157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979046-G-T

68875207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979096-G-A

68875222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979111-C-T

68875251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979132-G-C

68875251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979132-G-T

68875253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979134-A-T

68875300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979182-G-A

68875300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979182-G-T

http://identifiers.org/hco/3/GRCh38#68875308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96979190-A-C

68875381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979261-T-A

68875381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96979261-T-C

68875846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96981590-C-T

http://identifiers.org/hco/3/GRCh38#68875881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96981623-C-A

68875990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96981726-T-G

68876075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96981806-T-C

68876115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96982028-C-T

68876681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96982468-A-G

68876700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96982485-A-T

68877798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983151-G-A

68877798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983151-G-C

68877869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983225-T-C

68877879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983235-A-T

68878017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983373-C-T

68878091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983445-T-A

http://identifiers.org/hco/3/GRCh38#68878107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96983461-A-C

68878119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983472-G-A

68878188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983537-C-T

68878315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983673-G-A

68878463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96983818-T-C

68878688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96984018-G-A

68878800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96984130-A-G

68879181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96984980-C-T

68879182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96984981-G-A

http://identifiers.org/hco/3/GRCh38#68879238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96985035-C-A

68879238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96985035-C-T

68879564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96988740-C-T

68879595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96988771-A-G

68879751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96988925-G-A

68879776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96988950-T-C

68880385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991033-G-T

68880442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991044-C-T

68880597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991212-A-G

68880597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991212-A-T

68880634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991232-G-A

68880662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991260-A-T

68880665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991263-G-T

68880666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991264-T-C

68880674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991272-G-A

68880674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991272-G-C

68880681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991279-G-T

68880705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991308-T-A

68880705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991308-T-C

68880705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991308-T-G

68880796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: missense variant
orthologous variants: 96991399-C-G

68880810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: missense variant
orthologous variants: 96991413-T-G

68880907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991508-A-G

68880907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991508-A-T

68881025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991631-A-G

68881037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991643-G-C

68881223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96991831-G-A

68881773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96993937-A-G

68881906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96994062-A-G

68881931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96994081-T-C

68882404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96994708-G-A

68882495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96994790-G-A

68882668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96994948-C-T

68882825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995324-T-A

68882825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995324-T-C

68882918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995394-G-A

68883007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 96995447-G-T

68883143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995599-A-G

68883143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995599-A-T

68883190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96995649-G-A

http://identifiers.org/hco/3/GRCh38#68883480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96995918-A-C

68884669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96996119-G-A

68884669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96996119-G-T

http://identifiers.org/hco/3/GRCh38#68884877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96996410-C-A

68885107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96996796-T-A

68885153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96996845-G-A

68885153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96996845-G-T

68885217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 96996918-T-A

68885217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 96996918-T-C

http://identifiers.org/hco/3/GRCh38#68885246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96996947-A-C

68885283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 96996984-T-A

68885283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 96996984-T-G

68885385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997075-G-A

68885385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997075-G-C

68885391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997081-T-C

68885470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997142-A-G

http://identifiers.org/hco/3/GRCh38#68885595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96997892-A-C

68885665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997963-A-G

68885666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96997964-T-C

68885776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998002-A-G

68885838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998070-T-A

68885960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998187-C-T

http://identifiers.org/hco/3/GRCh38#68886037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96998315-C-A

http://identifiers.org/hco/3/GRCh38#68886125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96998417-A-C

http://identifiers.org/hco/3/GRCh38#68886223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96998508-C-A

68886360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998631-G-T

68886561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998810-T-C

68886613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96998875-A-T

http://identifiers.org/hco/3/GRCh38#68886733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#96998990-C-A

68886752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999009-G-T

68889125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999415-T-G

68889127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999417-G-C

68889152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999448-T-C

68889421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999724-G-A

68889421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999724-G-C

68889428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999731-T-C

68889598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 96999893-T-C

68890029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97000273-A-G

68890203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97000466-C-G

68890203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97000466-C-T

http://identifiers.org/hco/3/GRCh38#68890245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97000509-C-A

68890500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97000736-T-C

68890808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97001700-T-A

68890901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97001748-T-C

68891028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97001876-C-G

68891059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97001897-G-A

68891510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97002348-C-T

68891787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97002591-A-G

68893025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97003650-A-G

68893192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97003808-T-G

68893210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97003826-A-G

68893326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97003960-A-G

68893388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004018-G-C

68893388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004018-G-T

68893429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004069-G-A

68893434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004077-C-G

68893434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004077-C-T

http://identifiers.org/hco/3/GRCh38#68893513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97004143-A-C

68893553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004176-A-G

http://identifiers.org/hco/3/GRCh38#68893617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97004244-A-C

68893794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004416-T-C

68893794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97004416-T-G

68896033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97005665-A-G

68896103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97005709-G-A

68896106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97005712-G-A

68896106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97005712-G-C

68896106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97005712-G-T

68896675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006298-G-A

68896882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006500-T-C

68897934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006624-C-G

68897943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006633-T-A

68897943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006633-T-C

68897953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006642-T-C

68897959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006647-G-A

http://identifiers.org/hco/3/GRCh38#68898003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97006678-A-C

68898099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97006752-G-A

68898761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97007300-G-A

68900866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97007867-A-T

68901303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008262-C-G

68901303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008262-C-T

http://identifiers.org/hco/3/GRCh38#68901312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97008271-C-A

68901363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008325-G-C

68901388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008350-A-G

68901426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008386-C-G

68901483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97008439-T-G

http://identifiers.org/hco/3/GRCh38#68902212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97008835-A-C

68902703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009212-C-T

68903013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009543-T-A

68903013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009543-T-C

68903182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009692-C-T

68903396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009954-C-T

68903406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97009963-G-T

68904059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97011739-G-A

68904110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97011784-G-A

68904110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97011784-G-C

68904188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97011862-A-G

68904290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97011963-C-G

http://identifiers.org/hco/3/GRCh38#68904752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97012386-A-C

http://identifiers.org/hco/3/GRCh38#68904845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97012485-A-C

68904905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97012555-G-A

http://identifiers.org/hco/3/GRCh38#68905105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97012743-C-A

68905105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97012743-C-T

68905446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97012831-G-A

68906296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97013857-A-G

68906497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014050-A-T

68906580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014125-G-A

68906698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014241-C-T

http://identifiers.org/hco/3/GRCh38#68907093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97014285-C-A

68907145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014337-A-G

68907172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014360-G-C

68907601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014774-G-A

68907605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014778-T-A

68907605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014778-T-C

68907623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014796-G-A

68907714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014887-G-A

68907773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014951-C-T

68907774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014952-G-A

68907774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97014952-G-C

68907857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015019-A-G

68909983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015568-G-A

http://identifiers.org/hco/3/GRCh38#68910011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97015588-C-A

68910262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015808-A-G

68910268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015845-A-G

68910272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015849-G-T

68910281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015858-A-T

68910305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97015883-G-C

68910746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016250-A-T

68910815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016521-C-T

68910850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016556-A-G

68910860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016565-T-A

68911141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016806-C-T

68911151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97016816-G-A

http://identifiers.org/hco/3/GRCh38#68911256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97016922-A-C

http://identifiers.org/hco/3/GRCh38#68911541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97017260-A-C

68911886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97017631-G-A

68911963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97017711-A-G

68912069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97017822-T-C

68912069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97017822-T-G

68912200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97017960-G-T

68912327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018092-T-C

68912363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018128-T-C

68912438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018207-G-C

68912438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018207-G-T

68912549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018315-G-A

68912613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018381-T-C

68912635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018403-C-T

68912636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018404-G-A

68912636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018404-G-C

68912833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018595-A-G

68913012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018739-T-A

68913056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018787-C-T

68913058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018789-G-A

68913096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97018825-A-G

68913465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019154-T-C

68913536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019255-G-A

68913536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019255-G-T

68913579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019291-A-G

68914134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019785-T-C

68914158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97019809-C-G

68914584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97020275-C-T

68915273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97021060-A-G

68915479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97021106-G-T

68915952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97021488-C-T

http://identifiers.org/hco/3/GRCh38#68916332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97021845-C-A

68916582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97022164-T-C

http://identifiers.org/hco/3/GRCh38#68919236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#97023209-C-A

68919284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97023256-T-C

68919284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97023256-T-G

68919287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97023259-G-A

68919917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97024916-C-T

68919982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97024981-T-C

68920077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97025081-T-C

68920231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97025228-A-T

68920318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97025310-T-C

68920386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97025360-G-A

68920724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97025647-T-C

http://identifiers.org/hco/3/GRCh38#68920783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97025705-C-A

68920985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97026290-T-C

68921064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97026368-G-A

68921199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97026502-A-G

68921205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97026515-T-C

68921504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97027047-G-T

68921579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97027116-G-A

68921786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97027347-G-A

68921793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97027354-C-G

68921841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97027392-T-C

http://identifiers.org/hco/3/GRCh38#68922963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97028980-C-A

68922963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97028980-C-T

68923529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97029528-G-A

68923546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97029545-G-T

68923649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97029644-A-G

68923966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97029921-G-C

68924459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030636-G-T

68924505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030680-G-A

68924505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030680-G-C

68924540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030714-C-T

68924760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030935-A-G

68924769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030944-C-T

68924770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97030945-G-A

http://identifiers.org/hco/3/GRCh38#68927298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97033155-A-C

68927350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97033196-G-C

68927383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97033228-C-T

68928649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97033825-C-T

68928809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97033991-G-T

68928877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034063-G-A

68928877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034063-G-T

68929089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034273-G-A

68929089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034273-G-T

68929310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034462-A-G

68929333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034485-G-A

68929369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034497-T-A

68929369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034497-T-C

68929447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034543-C-T

68929538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034632-T-G

http://identifiers.org/hco/3/GRCh38#68929563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97034661-C-A

68929563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034661-C-T

68929708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034794-T-C

68929708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034794-T-G

68929721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034807-G-A

68929727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034812-T-C

68929727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034812-T-G

68929813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97034900-G-C

68930049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97035138-T-C

68930184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97035262-A-T

68930308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97035381-G-C

68931209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036174-A-G

68931276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036240-G-C

68931554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036474-G-A

68931554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036474-G-T

68931747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036624-C-T

68931851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036696-C-G

68932051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97036902-G-T

68932354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97037186-G-A

68932354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97037186-G-T

68932586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037413-G-A

68932586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037413-G-C

68932630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037457-T-A

68932630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037457-T-C

68932693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037527-T-C

http://identifiers.org/hco/3/GRCh38#68932709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#97037540-C-A

68932709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037540-C-G

68932709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037540-C-T

http://identifiers.org/hco/3/GRCh38#68932735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97037570-C-A

68932735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97037570-C-G

68932735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97037570-C-T

68932822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron_variant, undefined
orthologous variants: 97037660-A-G

68933269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97037994-G-A

68933346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038036-T-A

68933530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038209-G-A

68933708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038391-G-A

68933719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038402-C-T

68933720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038403-T-C

68933944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038640-C-T

68935291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038846-T-A

68935363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97038901-T-C

http://identifiers.org/hco/3/GRCh38#68935839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97039382-A-C

68935990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97039550-A-G

http://identifiers.org/hco/3/GRCh38#68936025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97039588-A-C

68936089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97039647-A-T

68936788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97040350-C-T

68936953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97040509-G-A

http://identifiers.org/hco/3/GRCh38#68936960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97040514-C-A

68936996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97040549-C-T

68937095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97040660-A-G

68937431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97040976-C-T

68937548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041092-G-A

http://identifiers.org/hco/3/GRCh38#68937602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97041146-A-C

68937602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041146-A-G

68937689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041211-C-G

http://identifiers.org/hco/3/GRCh38#68937841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97041362-C-A

68938062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041576-G-A

68938727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041723-A-G

68938952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97041937-T-A

http://identifiers.org/hco/3/GRCh38#68939058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97042040-C-A

68939058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042040-C-T

68939144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042103-T-C

68939238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042139-C-G

68939556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042182-A-G

68939562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042188-G-A

68939562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042188-G-C

http://identifiers.org/hco/3/GRCh38#68939634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97042248-C-A

68939634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042248-C-T

http://identifiers.org/hco/3/GRCh38#68939701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97042311-A-C

68939773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042386-C-T

68939849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042462-T-G

68940225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042792-A-T

68940351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042910-G-A

68940358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042917-G-T

68940420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97042975-G-A

68940758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97043315-C-T

68940847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97043403-A-G

68940848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97043404-A-G

68940895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97043449-G-C

68941203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97043985-C-T

68941314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97044092-A-G

68941552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97044304-A-T

68941711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97044428-G-A

68941729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97044446-A-G

68941734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97044451-G-C

http://identifiers.org/hco/3/GRCh38#68943738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97045922-A-C

68943983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97046167-T-A

http://identifiers.org/hco/3/GRCh38#68944162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97046310-A-C

68944178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97046324-A-G

68944527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97046728-T-C

68944527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97046728-T-G

http://identifiers.org/hco/3/GRCh38#68944694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97047012-C-A

68944694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97047012-C-G

68944694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97047012-C-T

68944893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97047219-T-G

http://identifiers.org/hco/3/GRCh38#68944903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97047229-C-A

68945141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97048208-G-A

68945361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97048406-G-C

68945419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97048465-T-G

68945930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97048988-T-C

68945971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97049031-A-G

68946347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97049863-A-G

68947278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97050411-A-G

68948255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97050969-G-C

68950012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97052780-C-G

68950149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97052923-T-C

68950527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97053310-C-G

68950565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97053349-C-G

68952355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97054934-C-T

68952479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97055044-G-A

68952567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97055131-G-A

68952567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97055131-G-T

68952593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97055156-T-C

68952611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: intron variant
orthologous variants: 97055174-T-A

68952703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97055277-T-A

68952786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056509-T-C

68952804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056527-T-G

http://identifiers.org/hco/3/GRCh38#68952862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97056602-C-A

68952862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056602-C-T

68953086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056843-T-C

68953095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056852-A-G

http://identifiers.org/hco/3/GRCh38#68953135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97056892-C-A

68953135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: 97056892-C-T

http://identifiers.org/hco/3/GRCh38#68953246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21591
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#97057001-C-A