23202561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3 prime UTR variant
orthologous variants: 19460482-A-G

23202619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3 prime UTR variant
orthologous variants: 19460541-G-A

23203437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461360-T-C

http://identifiers.org/hco/10/GRCh38#23203565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19461467-C-A

23203682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461509-G-T

23203788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461551-T-A

23203788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461551-T-C

23203833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461584-C-G

23203833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461584-C-T

23203869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461630-C-T

23203876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461637-G-T

23203997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461737-G-A

23203997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461737-G-C

23203998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461738-C-T

23204167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461882-G-A

23204167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 19461882-G-C

23204188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 19461903-T-C

23204194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 19461909-G-A

23204205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 19461920-G-A

23204205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 19461920-G-T

23204218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 19461933-C-T

23204316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462014-T-C

23204316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462014-T-G

23204317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462015-T-C

23204317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462015-T-G

http://identifiers.org/hco/10/GRCh38#23204320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19462020-C-A

23204320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462020-C-T

http://identifiers.org/hco/10/GRCh38#23204321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19462021-A-C

23204321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462021-A-G

23204321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462021-A-T

23204530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462210-A-G

23204602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462281-A-G

23204794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462457-T-C

23204950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462612-G-C

23205018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462681-C-T

23205019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462682-G-A

23205019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19462682-G-C

23205356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19463005-A-T

23205585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19463213-T-A

23205817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19463454-A-T

23206738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19464377-G-A

23206916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19464606-T-C

23207072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19464751-A-G

http://identifiers.org/hco/10/GRCh38#23207191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19464855-C-A

23207284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19464908-C-T

23208428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19466023-G-C

23208660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19466244-G-A

23208982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19466516-C-T

23209093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19466627-T-C

23218035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19475658-T-A

23218636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19475929-A-G

23218650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19475943-A-G

http://identifiers.org/hco/10/GRCh38#23219617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19477026-C-A

23219705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19477122-C-T

http://identifiers.org/hco/10/GRCh38#23219737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19477154-C-A

23219788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19477202-C-T

23220808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19477920-T-C

23220875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19477987-T-A

23220892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19478002-T-C

23221723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19478649-A-G

23221723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19478649-A-T

23221833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19478760-G-C

23222695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479076-G-A

23222697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479078-T-C

23222726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479107-C-T

http://identifiers.org/hco/10/GRCh38#23222997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19479915-A-C

23222997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479915-A-T

23223005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479923-G-A

23223005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479923-G-T

23223014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19479932-C-T

http://identifiers.org/hco/10/GRCh38#23223040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19479967-C-A

23223486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480075-A-G

23223486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480075-A-T

23223583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480355-A-G

23223588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480360-T-A

23223588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480360-T-C

23223633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 19480393-A-G

http://identifiers.org/hco/10/GRCh38#23223655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19480415-C-A

23223731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480491-A-G

23223864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480628-T-A

23223864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480628-T-C

http://identifiers.org/hco/10/GRCh38#23223881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19480645-C-A

23223881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480645-C-G

23223881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19480645-C-T

http://identifiers.org/hco/10/GRCh38#23223913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19480690-A-C

23223979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19481251-A-G

23239411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482279-C-T

http://identifiers.org/hco/10/GRCh38#23239465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19482332-C-A

23239612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482487-T-C

23239612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482487-T-G

23239636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482513-G-A

23239636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482513-G-C

23239636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482513-G-T

http://identifiers.org/hco/10/GRCh38#23239838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19482706-A-C

23239838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482706-A-G

23239854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482720-A-G

23239855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482721-A-T

23240284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19482843-C-T

23249466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484037-G-A

23249466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484037-G-T

23249467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484038-G-A

23249467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484038-G-C

23249765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484302-G-A

23250066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484851-G-A

23250115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19484898-G-A

23250487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 19485217-G-A

http://identifiers.org/hco/10/GRCh38#23250545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19485275-A-C

23250545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19485275-A-G

23250750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19485483-A-G

23253373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488487-G-A

23253516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488606-C-G

23253602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488687-A-G

23253655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488739-T-C

23253710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488789-A-G

23253730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488809-C-G

http://identifiers.org/hco/10/GRCh38#23253818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19488888-C-A

23253924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19488999-C-T

23254112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19489152-T-C

23254441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19489401-C-G

23254950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19489728-A-G

23261965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19492960-T-C

23262061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19493090-G-A

http://identifiers.org/hco/10/GRCh38#23262629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19493567-A-C

23262653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19493730-C-G

23262718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19493791-A-G

23263240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19494675-T-C

23263404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19494770-T-A

23263579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19494927-T-G

23264168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19495507-G-A

23264334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19495630-T-C

23264578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19495863-G-A

23264578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19495863-G-T

23264817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19496121-C-T

23265025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19497421-G-A

23265056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19497446-C-T

http://identifiers.org/hco/10/GRCh38#23265216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19497632-A-C

http://identifiers.org/hco/10/GRCh38#23265343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19497754-A-C

23265343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 19497754-A-T

23265417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19497817-G-A

23265443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19497845-G-C

23265495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19497876-G-C

23265596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498076-T-C

23265626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498125-C-T

23265799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498337-A-T

23266095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498614-G-C

http://identifiers.org/hco/10/GRCh38#23266138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19498647-C-A

23266138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498647-C-T

23266213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19498737-C-G

23266530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499130-T-C

23266531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499131-G-A

23266531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499131-G-T

23266736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499325-G-A

23266736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499325-G-C

23266812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499424-C-T

23267124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19499788-A-G

23267250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 19499935-T-C

23267250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 19499935-T-G

23268429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19500408-A-T

23268493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19500472-C-T

23280358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19514892-C-G

23280385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19514919-A-G

23280421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19514945-C-G

23280620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19515092-T-C

23280777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19515321-A-G

http://identifiers.org/hco/10/GRCh38#23280867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19515469-A-C

23280867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19515469-A-G

23281002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19515601-T-C

23281711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516281-G-T

23281739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516313-A-G

23281901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516471-G-A

http://identifiers.org/hco/10/GRCh38#23281913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19516483-C-A

23281913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516483-C-T

23281927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516501-A-G

23281937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 19516511-A-G

23282052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19516632-T-C

23282175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19516760-G-A

23282175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19516760-G-T

23282183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19516768-G-A

23282183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19516768-G-T

23283421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19517304-C-G

23283473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19517343-C-T

23283937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19517746-C-G

23284136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19517909-G-A

23284247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19517981-T-A

23285127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19518545-C-T

23285314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19518730-A-G

23285314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19518730-A-T

23285336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19518753-A-G

23285558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19519115-A-G

23285578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19519134-A-G

23286699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19519608-C-T

23286802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19519723-A-G

http://identifiers.org/hco/10/GRCh38#23288637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19519854-C-A

23289530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19520648-G-A

23289766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19520903-T-C

23289766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19520903-T-G

23289827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19520992-C-T

23289883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19521049-G-A

23290100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19521267-T-C

23290245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19521416-C-T

23290957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19522192-C-T

23291040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19522272-C-G

23291040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19522272-C-T

http://identifiers.org/hco/10/GRCh38#23291065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19522290-C-A

23291127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19522342-G-A

23291127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19522342-G-T

23292591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19523773-T-C

23292595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19523777-G-A

23292895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19524233-A-T

23292950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19524361-T-C

23292952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19524363-G-A

23292966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19524403-C-T

http://identifiers.org/hco/10/GRCh38#23293548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19525000-A-C

http://identifiers.org/hco/10/GRCh38#23293801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19525246-C-A

23293854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19525289-T-C

23293885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19525320-C-T

23293899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19525334-A-G

http://identifiers.org/hco/10/GRCh38#23294277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19525751-A-C

23294343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19525829-A-G

23294384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19525887-C-G

23294787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19526664-T-A

23294849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19526733-A-G

http://identifiers.org/hco/10/GRCh38#23302965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19528095-A-C

23303014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528138-T-C

23303173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528295-C-T

23303186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528308-T-A

23303186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528308-T-C

http://identifiers.org/hco/10/GRCh38#23303205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19528327-C-A

23303205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528327-C-T

http://identifiers.org/hco/10/GRCh38#23303239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19528699-C-A

23303239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528699-C-G

23303239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19528699-C-T

23303431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19528904-A-G

23303922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19529867-T-G

23304279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19530213-G-A

23304406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19530331-G-C

23313700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19532053-G-A

http://identifiers.org/hco/10/GRCh38#23313713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19532066-C-A

23313713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19532066-C-T

23315011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19533807-A-G

23315162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19533942-C-T

23315320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19534117-T-C

23315339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19534136-A-G

23315359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19534156-T-C

http://identifiers.org/hco/10/GRCh38#23319810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19537640-C-A

23319810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19537640-C-T

23319902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19537728-T-C

http://identifiers.org/hco/10/GRCh38#23320127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19537917-C-A

23320326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538133-G-A

23320686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538527-A-G

23320711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538552-A-G

23320711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538552-A-T

23320713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538554-A-G

23320851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538682-G-A

23320851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538682-G-C

23320851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538682-G-T

23320852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538683-T-C

http://identifiers.org/hco/10/GRCh38#23320913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19538744-A-C

23320913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19538744-A-G

23321375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19539248-T-G

23321419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19539292-C-T

http://identifiers.org/hco/10/GRCh38#23321516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19539352-A-C

23321586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19539419-A-G

23321587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19539420-G-A

http://identifiers.org/hco/10/GRCh38#23322303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19545001-C-A

23322303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19545001-C-T

http://identifiers.org/hco/10/GRCh38#23322340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19545027-C-A

23322508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19545194-C-T

23322545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19545232-T-C

23332816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19546621-G-A

23332944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19546954-T-A

23332944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19546954-T-C

23333077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19547201-C-T

23333176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19547300-G-A

23333196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19547320-A-T

23333265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19547370-A-T

http://identifiers.org/hco/10/GRCh38#23333281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19547386-A-C

23333281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19547386-A-G

23333381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19547483-C-T

23333587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19547653-C-G

23334328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19548225-A-G

23335789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552199-T-C

23335886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552269-C-T

23336111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552487-G-A

23336163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552534-G-A

23336298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552668-C-T

23336299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552669-G-A

23336299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19552669-G-T

23339213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554124-T-C

23339213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554124-T-G

23339730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554582-T-C

23339785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554639-A-G

23339893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554746-G-A

23340115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19554982-G-C

23340137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19555006-G-A

23340535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19555283-T-A

23340864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19555610-T-C

23341203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19555931-A-T

http://identifiers.org/hco/10/GRCh38#23341300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19556017-A-C

23341366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19556076-G-A

23342252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557013-T-C

23342263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557025-C-T

23342540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557319-T-G

23342940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557729-G-A

23342969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557753-T-C

23343029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19557810-A-T

23343255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19558064-A-T

23343375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19558187-G-A

23343670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19558455-G-A

23344037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 19558706-G-A

23344037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558706-G-C

23344037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558706-G-T

23344121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558773-G-A

23344121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558773-G-C

23344121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558773-G-T

23344232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19558800-G-T

23344344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19558834-G-A

23344419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 19558902-T-A

23344419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 19558902-T-C

23344472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19558975-A-G

23344472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28716
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19558975-A-T