72044419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110311696-C-T

72044911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110311279-A-G

72044994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110311361-A-G

72045004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110311371-C-G

72045004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110311371-C-T

72053560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110306978-G-A

72053651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110306901-C-T

http://identifiers.org/hco/16/GRCh38#72054129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110306470-C-A

http://identifiers.org/hco/16/GRCh38#72054259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110306343-C-A

72054443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110305899-A-G

72054568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110305765-A-G

72054572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110305761-G-A

72054572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110305761-G-T

72054575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110305758-A-G

72054580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110305748-T-C

72054608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110305695-C-G

72054617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110305685-C-T

http://identifiers.org/hco/16/GRCh38#72055909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110304415-C-A

http://identifiers.org/hco/16/GRCh38#72055971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110304375-C-A

72055971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110304375-C-T

72056003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110304343-T-C

72056027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110304324-G-A

72056075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110304276-G-A

72056094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110304252-T-G

72056217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 110304136-C-G

72056217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110304136-C-T

72056229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110304124-T-C

72056402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303981-T-C

72056435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303950-T-C

72056445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303940-G-A

72056445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303940-G-C

72056445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303940-G-T

72056705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303699-G-T

72056727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303677-G-A

72057409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110303392-G-A

http://identifiers.org/hco/16/GRCh38#72057511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110303303-A-C

72057511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303303-A-G

72057547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303278-G-A

72057547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303278-G-T

72057581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303272-G-A

72057623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303239-T-A

72057629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303233-G-C

72057629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303233-G-T

72057659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303206-G-T

http://identifiers.org/hco/16/GRCh38#72057752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110303126-C-A

72057752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303126-C-T

72057758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303120-G-A

72057758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303120-G-T

72057856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303013-C-T

72057858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303011-T-A

72057858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303011-T-C

72058008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302919-G-A

72058429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303699-G-A

72058451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303677-G-A

72058479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110303648-G-T

72059131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110303392-A-G

http://identifiers.org/hco/16/GRCh38#72059202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110303321-A-C

72059226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303303-A-G

72059262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303278-G-A

72059338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303239-T-A

72059338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303239-T-C

72059344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303233-G-T

72059365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303215-A-G

72059374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303206-G-T

72059466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303126-G-T

72059472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303120-G-T

72059491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110303095-T-G

72059723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110302919-G-A

72059817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110302907-G-C

72059817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110302907-G-T

72059818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110302906-G-T

72059881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302848-T-C

72059920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302844-T-C

72059920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302844-T-G

72059980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302814-A-G

72060031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: 110302763-G-A

http://identifiers.org/hco/16/GRCh38#72060074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302715-C-A

72060105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 110302686-T-C

72060156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 110302635-C-T

72060189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302602-C-T

72060198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302593-G-T

72060205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302586-T-C

72060207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302584-G-T

72060216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302575-C-T

72060217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302574-A-G

72060218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302573-T-A

72060219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302572-A-T

72060228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 110302563-A-G

72060231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302560-G-T

72060238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302553-C-T

http://identifiers.org/hco/16/GRCh38#72060252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302539-C-A

72060270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302521-G-A

72060319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302472-T-C

72060354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302437-C-G

72060357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302434-C-T

72060381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 110302410-C-T

72060447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302344-G-A

72060447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302344-G-C

http://identifiers.org/hco/16/GRCh38#72060498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302293-C-A

72060498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302293-C-T

72060522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302269-G-A

http://identifiers.org/hco/16/GRCh38#72060525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302266-C-A

72060525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 110302266-C-T

http://identifiers.org/hco/16/GRCh38#72060551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302240-C-A

http://identifiers.org/hco/16/GRCh38#72060555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302236-C-A

72060579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302212-G-A

72060612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302179-G-A

72060612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302179-G-T

72060638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 110302153-A-G

72060672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 110302119-A-G

72060684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302107-T-C

72060696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302095-A-G

72060697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302094-T-A

72060708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_gained, undefined
orthologous variants: 110302083-C-T

72060729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302062-G-A

72060729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302062-G-T

72060732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302059-G-A

72060748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302043-C-T

72060756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302035-G-A

72060756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302035-G-C

http://identifiers.org/hco/16/GRCh38#72060757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302034-A-C

72060780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302011-G-T

http://identifiers.org/hco/16/GRCh38#72060781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302010-C-A

72060781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302010-C-G

72060781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110302010-C-T

72060792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 110301999-T-C

72060792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301999-T-G

72060801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301990-G-A

72060801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301990-G-C

72060810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301981-T-C

72060816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301975-G-A

72060846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301945-A-G

72061039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110301775-A-G

72063171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305765-A-G

72063175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305761-G-C

72063175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305761-G-T

72063178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305758-A-G

72063178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305758-A-T

72063183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305748-T-G

72063211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305695-C-G

72063211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110305695-C-T

72073748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110304324-G-T

72073796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110304276-G-A

72073821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110304252-T-C

72073821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110304252-T-G

72074431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303719-T-G

72074458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303699-G-A

72074458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303699-G-C

72074458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303699-G-T

72074480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303677-G-A

72074480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303677-G-T

72074505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303651-T-C

72074508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303648-G-T

72074572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303585-T-A

72074572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110303585-T-C

72075162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110303392-G-A

72075162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110303392-G-T

72075233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303321-A-G

http://identifiers.org/hco/16/GRCh38#72075264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110303303-A-C

72075264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303303-A-G

72075300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303278-G-A

72075300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303278-G-T

72075334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303272-G-T

72075376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303239-T-C

72075411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303206-G-C

72075610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110303011-T-C

72076134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110302848-T-A

72076164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110302821-G-C

72076165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110302820-A-G

72076222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110302763-G-C

72076245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110302743-C-T

http://identifiers.org/hco/16/GRCh38#72076265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302715-C-A

72076296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110302686-T-C

72076380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302602-C-T

72076396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, start_lost
orthologous variants: 110302586-T-A

72076396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, start_lost
orthologous variants: 110302586-T-C

72076398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302584-G-C

72076398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302584-G-T

72076403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 110302579-C-G

72076403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 110302579-C-T

72076407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302575-C-T

72076408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302574-A-G

72076410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302572-A-T

72076419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302563-A-T

72076429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302553-C-T

72076440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302542-G-A

http://identifiers.org/hco/16/GRCh38#72076443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302539-C-A

72076443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302539-C-G

72076443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 110302539-C-T

72076458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302524-A-T

72076461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302521-G-C

72076510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302472-T-A

72076510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302472-T-C

72076530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302452-T-C

72076548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302434-C-T

72076551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302431-G-A

72076551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302431-G-C

http://identifiers.org/hco/16/GRCh38#72076572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302410-C-A

72076572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 110302410-C-T

72076638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302344-G-A

72076675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302307-A-G

http://identifiers.org/hco/16/GRCh38#72076689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302293-C-A

72076689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302293-C-T

72076713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302269-G-A

72076713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302269-G-C

http://identifiers.org/hco/16/GRCh38#72076716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302266-C-A

72076725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302257-A-G

http://identifiers.org/hco/16/GRCh38#72076737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302245-A-C

http://identifiers.org/hco/16/GRCh38#72076742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302240-C-A

72076742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 110302240-C-T

72076746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302236-C-G

72076746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 110302236-C-T

72076770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302212-G-A

72076863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302119-A-T

72076885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302097-G-C

72076887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302095-A-G

72076888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302094-T-C

72076888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302094-T-G

72076890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302092-T-C

http://identifiers.org/hco/16/GRCh38#72076899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110302083-C-A

72076899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302083-C-G

72076914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302068-T-A

72076914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302068-T-C

72076917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302065-G-T

72076920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302062-G-A

72076923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302059-G-A

72076923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302059-G-T

72076944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302038-C-T

72076947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302035-G-A

72076947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302035-G-T

72076948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 110302034-A-G

72076968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302014-T-C

72076971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302011-G-A

72076971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302011-G-C

72076971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302011-G-T

72076972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 110302010-C-T

72076981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110302001-T-A

72076981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 110302001-T-C

72076983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 110301999-C-T

72076992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301990-G-A

72076992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 110301990-G-C

72077007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 110301975-G-A

http://identifiers.org/hco/16/GRCh38#72077037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110301945-A-C

72077731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110301429-G-A

72084752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110300751-T-C

72084760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: intron variant
orthologous variants: 110300742-C-T

72084909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300625-A-G

72084936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300598-C-G

http://identifiers.org/hco/16/GRCh38#72085145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110300459-A-C

http://identifiers.org/hco/16/GRCh38#72085146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110300458-C-A

72085159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110300446-G-A

72085159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 110300446-G-T

http://identifiers.org/hco/16/GRCh38#72085169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110300436-C-A

72085169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 110300436-C-T

72085172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 110300433-T-C

72085174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 110300431-T-C

72085178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 110300427-G-A

72085178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 110300427-G-C

72085183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 110300422-A-G

72085183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 110300422-A-T

72085184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300421-G-T

72085188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300417-A-G

72085252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300353-G-A

72085252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300353-G-T

72085308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300311-T-C

http://identifiers.org/hco/16/GRCh38#72085312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110300307-C-A

72085349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300272-T-C

72085385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300238-T-A

72085385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300238-T-C

72085386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300237-A-G

72085386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300237-A-T

72085476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300159-T-A

72085535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300112-G-A

72085590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300070-C-G

72085590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300070-C-T

http://identifiers.org/hco/16/GRCh38#72085593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110300067-C-A

72085593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300067-C-T

72085624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110300040-G-A

http://identifiers.org/hco/16/GRCh38#72086420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110299693-C-A

72086420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299693-C-G

72086420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299693-C-T

72086452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299661-G-A

72086497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299621-G-A

72086497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299621-G-T

http://identifiers.org/hco/16/GRCh38#72086589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#110299530-C-A

72086589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299530-C-G

72086589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 110299530-C-T

72086899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110299243-T-C

72086899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110299243-T-G

72086904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110299238-T-C

72087155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110299027-A-G

72087306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110298880-C-T

72087336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110298850-G-A

72087336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110298850-G-T

72087459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298575-T-G

72087511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298523-G-T

72087559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298475-A-T

72088398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298333-T-A

72088442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298290-G-A

72088541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298197-T-C

72088975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110298164-A-G

72089166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110297973-A-G

72089849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110296679-G-A

72089849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110296679-G-T

72089894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110296637-T-C

72089943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110296588-G-T

72090102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110296238-A-T

72090283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295988-T-C

72090283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295988-T-G

http://identifiers.org/hco/16/GRCh38#72090308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110295980-A-C

72090425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295892-C-T

72090440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295877-C-G

http://identifiers.org/hco/16/GRCh38#72090526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110295798-C-A

72090526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295798-C-T

72090555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295783-A-G

http://identifiers.org/hco/16/GRCh38#72090570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110295769-A-C

72090851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295506-A-T

http://identifiers.org/hco/16/GRCh38#72090863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110295493-A-C

http://identifiers.org/hco/16/GRCh38#72090878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110295476-C-A

72090878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295476-C-G

72091318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110295041-G-A

72091386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110294977-T-C

http://identifiers.org/hco/16/GRCh38#72092001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110294416-A-C

http://identifiers.org/hco/16/GRCh38#72092077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110294329-A-C

72092585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110293626-T-G

72092617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110293596-T-A

72093530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292665-C-G

72093547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292623-G-A

72093547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292623-G-C

72093547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292623-G-T

72093624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292547-G-A

72093647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 110292521-T-C

72093670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292495-G-T

72093675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292490-C-T

http://identifiers.org/hco/16/GRCh38#72093716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110292447-C-A

72093716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292447-C-T

72093731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292432-G-A

72093731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110292432-G-T

72093865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292306-G-A

72093900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110292272-G-C

72094059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110292113-T-C

72094059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110292113-T-G

72094060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110292112-C-T

http://identifiers.org/hco/16/GRCh38#72094077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110292095-C-A

72094077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110292095-C-T

72094124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110292048-C-T

72094161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110292012-T-C

72094199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110291976-G-T

72094203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110291972-G-A

72094203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110291972-G-T

http://identifiers.org/hco/16/GRCh38#72094322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#110291865-C-A

72094398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26041
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110291790-G-A