http://identifiers.org/hco/10/GRCh38#75099602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21791667-C-A

75099602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21791667-C-T

75099648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21791691-T-C

75099896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791872-C-G

75099896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21791872-C-T

http://identifiers.org/hco/10/GRCh38#75100005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21791968-C-A

75100060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21792027-G-C

75100067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21792034-G-A

75100120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21792083-C-T

75100392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792278-T-C

75100608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792443-C-T

75100749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792560-G-A

75100781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21792592-G-A

http://identifiers.org/hco/10/GRCh38#75100890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21792683-A-C

75101296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793019-C-T

75101349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793069-T-C

75101394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793114-A-G

http://identifiers.org/hco/10/GRCh38#75101765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21793411-A-C

75101801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793451-G-T

75101858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793494-C-T

http://identifiers.org/hco/10/GRCh38#75101879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21793515-C-A

75101883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21793519-C-G

75101886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21793522-A-G

75101920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21793556-G-A

75101964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 21793600-A-G

75101971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793607-G-T

75102174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793806-T-G

75102200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793836-G-C

75102212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793848-G-C

75102214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793850-A-T

75102312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793944-G-A

75102313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21793945-G-C

75103144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794245-A-G

75103705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794710-A-G

75103746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794717-G-A

75103746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794717-G-T

75103882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794804-G-A

75103882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21794804-G-T

75103901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794823-G-A

75103901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794823-G-T

75103913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794835-T-C

75103929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794851-T-C

75103934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794856-G-A

75103934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794856-G-T

75103948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21794870-G-A

75103948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21794870-G-T

75103954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21794876-G-A

http://identifiers.org/hco/10/GRCh38#75103958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21794880-C-A

75103958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794880-C-G

75103958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794880-C-T

75103960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21794882-G-A

75103989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21794911-C-T

75104076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, start_lost
orthologous variants: 21794989-T-A

75104076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, start_lost
orthologous variants: 21794989-T-C

75104165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795076-G-C

75104165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795076-G-T

75104197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795108-T-G

75104207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795122-A-T

75104250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21795164-T-A

75105588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796302-T-A

75105633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796347-C-T

http://identifiers.org/hco/10/GRCh38#75105680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21796397-C-A

75105680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21796397-C-T

http://identifiers.org/hco/10/GRCh38#75105748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21796465-C-A

75105748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 21796465-C-T

75105963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796660-G-T

75106121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796766-T-A

75106121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796766-T-C

75106133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796774-A-G

75106133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21796774-A-T

75106510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797016-T-A

75106510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797016-T-C

75106520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797026-A-G

75106673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797162-C-T

75106853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797335-G-A

75107988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797485-C-T

75108149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21797646-G-A

75108149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21797646-G-T

75108152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21797649-G-A

75108152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21797649-G-C

75108152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 21797649-G-T

75108271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21797767-G-A

75108271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21797767-G-T

75108343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797837-G-A

75108343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797837-G-T

http://identifiers.org/hco/10/GRCh38#75108428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21797912-C-A

75108495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21797974-C-T

http://identifiers.org/hco/10/GRCh38#75108954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798462-A-C

75108961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798469-G-A

75108961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798469-G-T

http://identifiers.org/hco/10/GRCh38#75108963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798471-C-A

75108963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798471-C-G

75108963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798471-C-T

75109009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 21798514-G-A

75109017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 21798522-T-C

http://identifiers.org/hco/10/GRCh38#75109165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798670-C-A

75109165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798670-C-T

http://identifiers.org/hco/10/GRCh38#75109173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798678-C-A

75109173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21798678-C-T

http://identifiers.org/hco/10/GRCh38#75109206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798704-C-A

http://identifiers.org/hco/10/GRCh38#75109317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798811-C-A

75109317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, undefined
orthologous variants: 21798811-C-T

http://identifiers.org/hco/10/GRCh38#75109362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21798852-C-A

75109362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21798852-C-T

75109485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21798971-T-C

75109705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21799153-A-G

75110630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21799971-T-G

75110716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800060-C-G

75111228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800413-T-C

75111266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800454-G-A

75111395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800565-T-C

75111472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800599-G-A

75111472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron variant
orthologous variants: 21800599-G-T

75111522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21800649-G-A

75111522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 21800649-G-T

http://identifiers.org/hco/10/GRCh38#75111592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21800718-C-A

75111592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, missense_variant
orthologous variants: 21800718-C-T

75111596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21800722-G-A

75111596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21800722-G-C

75111596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 21800722-G-T

75111621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 21800747-G-A

75111621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, stop_gained, undefined
orthologous variants: 21800747-G-T

75111623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 21800749-G-A

75111623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 21800749-G-T

75111650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 21800776-G-A

75111650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 21800776-G-T

75111772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21800898-G-A

75111772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21800898-G-T

75112281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21801295-C-T

75112296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21801310-T-C

75112349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21801347-A-G

75112789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21801735-C-G

75113564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21802329-T-C

75113629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21802399-A-G

75113720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21802484-G-T

75114395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21802988-A-G

75114579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21803153-T-A

75114747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21803406-G-A

75114747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21803406-G-C

75117908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21803898-T-C

http://identifiers.org/hco/10/GRCh38#75118038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21804011-A-C

75118062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21804039-A-G

75118333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21804278-A-G

75119623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21806298-C-G

75138602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21815307-C-G

75138788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21816198-C-T

http://identifiers.org/hco/10/GRCh38#75146788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21822500-A-C

75146793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21822505-C-T

75146915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21822628-G-A

75146915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21822628-G-T

75147080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21822786-C-G

75147080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21822786-C-T

75147773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823124-G-T

75148190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823302-C-T

75148289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823401-G-T

75148757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823552-T-C

75149017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823762-G-A

75149050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21823796-T-G

75149334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824065-A-G

75149411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824125-C-T

75149427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824141-A-G

http://identifiers.org/hco/10/GRCh38#75149467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21824165-C-A

75149728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824550-T-C

75150475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21824992-C-G

75150501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21825018-T-G

75150519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 21825036-G-A

75150767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 21825284-T-C

75150767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 21825284-T-G

75150864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21825381-T-C

75151026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21825543-A-G

75151026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21825543-A-T

75151153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21825668-T-A

75164489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830008-A-T

75164508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830029-C-T

75164678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21830187-G-A

75164678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21830187-G-C

75164684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21830193-A-G

75164735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 21830244-G-A

75164735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 21830244-G-C

http://identifiers.org/hco/10/GRCh38#75164752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21830261-C-A

75164752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830261-C-T

75164774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830279-T-C

http://identifiers.org/hco/10/GRCh38#75164783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21830288-C-A

75164783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830288-C-T

http://identifiers.org/hco/10/GRCh38#75164789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21830293-C-A

75164789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830293-C-T

75164790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830294-A-G

75164792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830296-G-T

75164804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830307-T-G

75164890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21830378-A-G

75166430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21831262-A-G

75166464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21831295-T-C

75166602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831416-A-G

75166818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831790-A-G

75166855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21831827-G-A

75168529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 21833734-G-T

75168544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21833750-A-G

75168544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 21833750-A-T

75168677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21833883-T-C

http://identifiers.org/hco/10/GRCh38#75168766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21834010-C-A

75168771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834015-A-G

http://identifiers.org/hco/10/GRCh38#75168775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21834019-C-A

75168775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21834019-C-T

75170411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21835052-C-T

75172952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21839691-G-A

75172990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21839744-T-C

75173091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21839850-T-G

75173361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21840123-C-T

75175811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21842190-A-T

75175818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 21842197-G-T

75176264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21842670-G-A

75176293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21842751-T-G

75176343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 21842957-T-C

75176400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 21843017-G-A

75176916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843526-T-C

75176937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843547-G-T

75176957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843566-G-A

75176978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843587-T-C

http://identifiers.org/hco/10/GRCh38#75177125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21843704-C-A

75177242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843812-A-G

75177267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21843826-G-T

75177586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844131-G-A

75178062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844599-T-C

75178085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844620-C-T

75178248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844778-T-A

75178281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844807-A-G

http://identifiers.org/hco/10/GRCh38#75178314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#21844848-C-A

75178394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844933-G-T

75178396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21844935-A-G

75179402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21845173-T-C

75179496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21845273-G-A

75179508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21845285-G-A

75179508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21845285-G-T

75179849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 21845532-T-G

75180294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21845918-G-T

http://identifiers.org/hco/10/GRCh38#75180876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#21846306-C-A

75180982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21846391-G-A

75181062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21846463-G-T

75181091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21846484-G-T

75181120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21846510-G-T

75181135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21846524-C-T

75181458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21848143-A-G

75182073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26320
most severe consequence: 3 prime UTR variant
orthologous variants: 21848743-G-A