74330325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99928066-A-G

74330554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99927867-C-T

http://identifiers.org/hco/11/GRCh38#74330612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99927812-C-A

74330910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99927107-G-C

74331224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926778-G-A

74331253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926757-G-T

http://identifiers.org/hco/11/GRCh38#74331824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99926402-C-A

74331830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926396-C-T

74331932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926297-T-C

74332122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926147-C-G

74332126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99926143-A-G

http://identifiers.org/hco/11/GRCh38#74332192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99925951-C-A

74332192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925951-C-T

http://identifiers.org/hco/11/GRCh38#74332315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99925825-C-A

74332600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925558-T-G

74332670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925496-T-A

74332670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925496-T-C

74332990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925225-T-C

http://identifiers.org/hco/11/GRCh38#74332992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99925223-C-A

74332992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99925223-C-T

74333307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924756-T-A

74333309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924754-C-G

74333309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924754-C-T

74333416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924653-T-C

74333546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924526-C-T

http://identifiers.org/hco/11/GRCh38#74333725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99924352-C-A

http://identifiers.org/hco/11/GRCh38#74333818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99924171-C-A

74333818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924171-C-T

74333821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924160-T-A

74333908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99924075-A-G

http://identifiers.org/hco/11/GRCh38#74333954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99924024-C-A

http://identifiers.org/hco/11/GRCh38#74334087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99923904-C-A

http://identifiers.org/hco/11/GRCh38#74334159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99923823-C-A

74334159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923823-C-T

74334178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923804-T-C

74334238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923748-T-A

74334260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923727-A-G

74334273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923714-T-C

74334326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923659-A-G

74334376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923622-T-C

74334438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923576-A-G

74334505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923506-T-C

74334550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923466-C-T

74334560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923465-G-A

74334626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923401-T-A

74334636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923393-A-G

74334688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923342-G-A

74334688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923342-G-T

http://identifiers.org/hco/11/GRCh38#74334692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99923338-C-A

74334692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923338-C-T

74334966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923187-G-T

http://identifiers.org/hco/11/GRCh38#74334980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99923180-C-A

74334980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99923180-C-T

74335575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922847-T-G

74335768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922663-T-C

74335959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922483-T-C

74335959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922483-T-G

http://identifiers.org/hco/11/GRCh38#74336096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99922349-C-A

74336127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922320-T-A

74336141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922309-C-T

74336229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99922020-G-T

74336339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99921921-T-C

74336344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99921916-T-A

74336344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99921916-T-C

http://identifiers.org/hco/11/GRCh38#74336600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99921685-C-A

74336600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99921685-C-T

http://identifiers.org/hco/11/GRCh38#74336624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99921661-C-A

74336624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99921661-C-T

74336710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99921576-G-A

74336782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99921501-T-G

74337213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920984-G-C

74337302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920900-A-T

74337307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920895-C-T

74337324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920878-T-C

http://identifiers.org/hco/11/GRCh38#74337427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99920792-C-A

74337427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920792-C-G

74337427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920792-C-T

74337568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920668-T-C

74337903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920366-A-G

74338000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99920272-T-A

http://identifiers.org/hco/11/GRCh38#74338352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99919778-C-A

74338416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919717-T-C

74338440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919693-T-C

74338440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919693-T-G

74338445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919688-A-G

74338477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99919657-G-A

74338477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99919657-G-T

74338680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919476-T-C

74338734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919425-G-C

74338734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919425-G-T

74340567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99919097-A-T

74340753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99918911-T-C

http://identifiers.org/hco/11/GRCh38#74341056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99918301-A-C

http://identifiers.org/hco/11/GRCh38#74341121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99918236-C-A

74341170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99918178-T-C

74341178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99918170-T-C

74341266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99918089-C-T

74342313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917655-T-C

http://identifiers.org/hco/11/GRCh38#74342373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99917599-C-A

74342373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917599-C-G

74342409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917562-A-T

74342690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917284-A-T

http://identifiers.org/hco/11/GRCh38#74342698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99917277-A-C

74342698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917277-A-G

74342698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917277-A-T

74342736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99917243-A-G

74342840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916873-T-G

74342961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99916744-C-T

74343022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 99916683-T-C

74343026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916679-A-G

74343059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916647-T-C

74343061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916645-T-C

http://identifiers.org/hco/11/GRCh38#74343113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99916597-A-C

http://identifiers.org/hco/11/GRCh38#74343225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99916064-C-A

74343225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916064-C-T

74343231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916058-A-G

74343238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99916052-A-G

http://identifiers.org/hco/11/GRCh38#74343254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99916036-C-A

74343492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915799-T-C

74343502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915789-G-A

74343502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915789-G-T

http://identifiers.org/hco/11/GRCh38#74343560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99915734-C-A

74343560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915734-C-T

http://identifiers.org/hco/11/GRCh38#74343598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99915696-C-A

74343756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915562-T-G

74344556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99915132-C-T

http://identifiers.org/hco/11/GRCh38#74344888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99912882-A-C

74345130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99912645-C-G

74345179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99912612-G-A

74345384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99912382-A-G

74345384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99912382-A-T

74345398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99912369-T-C

74345642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99912123-A-G

74345786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99911978-T-A

74346863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99911236-G-T

74346912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99911187-G-A

74346912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99911187-G-T

74346916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99911183-T-C

74347290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99910852-T-C

74347360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99910783-G-T

http://identifiers.org/hco/11/GRCh38#74347370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99910773-A-C

74347370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99910773-A-G

74351347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99909313-C-G

74351413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 99909252-A-G

http://identifiers.org/hco/11/GRCh38#74351636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99909017-C-A

74351835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99908884-G-A

74351979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99908746-A-T

74352390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99907836-T-C

74367855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99905411-A-G

74367880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99905387-T-C

74367984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99905290-G-A

74367984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, undefined
orthologous variants: 99905290-G-T

http://identifiers.org/hco/11/GRCh38#74368347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99904952-C-A

http://identifiers.org/hco/11/GRCh38#74368360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99904939-C-A

74368420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99904887-T-C

74368477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99904837-G-A

74370889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99902535-A-G

http://identifiers.org/hco/11/GRCh38#74370918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99902506-A-C

http://identifiers.org/hco/11/GRCh38#74371005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99902421-A-C

74371067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99902361-A-G

http://identifiers.org/hco/11/GRCh38#74371134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99902197-A-C

74371135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99902196-T-C

74371226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901959-C-T

74371228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901957-C-T

74371465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901754-T-C

http://identifiers.org/hco/11/GRCh38#74371590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99901606-C-A

74371590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901606-C-T

74371595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901601-G-A

74371595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901601-G-T

74371623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901575-T-G

74371703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99901504-C-T

http://identifiers.org/hco/11/GRCh38#74371768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99901439-C-A

http://identifiers.org/hco/11/GRCh38#74371840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99901372-A-C

74371868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901241-T-C

74371921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901199-G-A

74371921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99901199-G-T

74372154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99900977-A-G

74372184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99900948-G-A

74373307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99898872-T-C

74374467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: missense variant
orthologous variants: 99899612-A-G

http://identifiers.org/hco/11/GRCh38#74374503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99899576-C-A

74374503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: missense variant
orthologous variants: 99899576-C-T

74374669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99899415-C-G

74374724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99899313-T-A

74375593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99898243-A-G

74375603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99898233-A-T

74375984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99897700-A-G

74375991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99897693-A-G

74376146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99897542-C-T

http://identifiers.org/hco/11/GRCh38#74376710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99897190-A-C

http://identifiers.org/hco/11/GRCh38#74376992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99896890-A-C

74377369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99896733-A-G

74377577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99896637-T-C

74377635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99896558-G-A

74377635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99896558-G-C

74378853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99895551-C-G

74378853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99895551-C-T

74378867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99895541-G-A

74379999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99894778-C-T

http://identifiers.org/hco/11/GRCh38#74380329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99894517-A-C

74381786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99893528-T-C

74381850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99893469-A-G

74381910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99893410-C-T

74388667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99884190-A-G

74388785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99883736-T-C

74391186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99882126-G-A

74391186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99882126-G-T

74393642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99880710-C-T

http://identifiers.org/hco/11/GRCh38#74394329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99880046-A-C

74394611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99879608-T-A

74394818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99879387-A-G

74394961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99879250-C-G

74395933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: -T-C

74396766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99878570-A-G

http://identifiers.org/hco/11/GRCh38#74396788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99878550-C-A

74397118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99878194-A-G

74397176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99878150-C-T

74397231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99878095-T-C

http://identifiers.org/hco/11/GRCh38#74397521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877777-C-A

74397521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99877777-C-G

74397521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron variant
orthologous variants: 99877777-C-T

http://identifiers.org/hco/11/GRCh38#74397565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877733-A-C

74397565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877733-A-G

74397565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877733-A-T

74397585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877703-G-A

74397585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877703-G-T

http://identifiers.org/hco/11/GRCh38#74397588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877700-A-C

74397588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877700-A-G

74397588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877700-A-T

74397657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877642-A-G

http://identifiers.org/hco/11/GRCh38#74397782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877513-A-C

74397782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877513-A-G

http://identifiers.org/hco/11/GRCh38#74397795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877500-A-C

74397795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877500-A-G

74397795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877500-A-T

74397863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877431-G-A

74397884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877410-G-A

74397884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99877410-G-T

http://identifiers.org/hco/11/GRCh38#74397941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877353-C-A

74397941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877353-C-G

74397941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877353-C-T

http://identifiers.org/hco/11/GRCh38#74398172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877118-C-A

74398172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99877118-C-T

http://identifiers.org/hco/11/GRCh38#74398201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#99877087-C-A

74398386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20898
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 99876903-G-T