http://identifiers.org/hco/2/GRCh38#27781489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31781712-C-A

http://identifiers.org/hco/2/GRCh38#27781558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31781769-C-A

27781558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31781769-C-T

http://identifiers.org/hco/2/GRCh38#27781828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31782039-C-A

http://identifiers.org/hco/2/GRCh38#27781832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31782043-C-A

27781850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31782074-A-G

27781881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31782138-A-G

27781890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31782147-T-C

27782006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31782243-C-T

27794534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31783292-T-C

27795673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31784305-G-A

27795707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31784324-C-T

27795708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31784325-C-T

27796038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31784628-T-G

27796847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31785692-G-A

http://identifiers.org/hco/2/GRCh38#27797092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31785938-A-C

http://identifiers.org/hco/2/GRCh38#27797771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31786962-A-C

27797876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31787065-C-G

27797884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31787073-G-A

27798024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31787178-G-T

27799107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31787309-C-T

27800487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31788370-G-A

27800837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31788660-C-T

27801283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789668-T-C

27801302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789691-C-G

27802484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789827-G-A

27802486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789829-G-T

27802515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789856-G-T

27802535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789873-G-T

27802632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31789966-G-A

27802955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31790236-C-T

27803253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31790365-A-G

27804261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31790822-A-G

27804261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31790822-A-T

27804566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791049-C-T

27804568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791051-A-G

27804617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791091-G-A

27804695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791167-T-C

27805313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791332-G-A

27805361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791377-C-G

http://identifiers.org/hco/2/GRCh38#27805412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31791428-A-C

27805432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791429-C-T

27805437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791434-C-T

27805442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791439-G-A

27805488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791483-G-A

27806297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791645-C-T

27806304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791657-A-T

http://identifiers.org/hco/2/GRCh38#27806351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31791704-A-C

27806508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791851-G-A

27806518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791854-T-C

27806531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791867-T-C

27806580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791889-G-A

27806697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791980-C-T

27806711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31791994-T-C

27806832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31792114-C-T

27807111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31792349-G-A

27807743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31792753-T-G

27807885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31792930-A-G

http://identifiers.org/hco/2/GRCh38#27807970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31793013-A-C

27807970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793013-A-G

http://identifiers.org/hco/2/GRCh38#27807993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31793036-A-C

27808001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793044-G-A

27808021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793064-G-A

27808155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793187-A-G

27808459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793434-G-A

27808470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793444-C-T

27808647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31793564-G-A

27809428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794010-A-G

27809495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794072-G-A

27809495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794072-G-C

27809497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794074-G-T

27809564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794153-T-C

http://identifiers.org/hco/2/GRCh38#27809786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31794348-A-C

27809808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31794370-A-T

27809833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31794395-T-C

http://identifiers.org/hco/2/GRCh38#27809843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31794405-C-A

http://identifiers.org/hco/2/GRCh38#27809854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31794416-C-A

27809854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 31794416-C-G

27810232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31794769-G-A

http://identifiers.org/hco/2/GRCh38#27810468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31795041-A-C

27814930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31795822-C-G

27814974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31795847-C-G

27815020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31795887-C-T

27815123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31795976-C-T

27815147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31795993-T-C

27815157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31796003-T-A

27816053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31796205-C-T

27816383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31796519-C-G

27816433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31796576-G-C

27816945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31797538-A-G

27817039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31797613-C-T

27817143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31797720-G-T

27817154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31797730-A-G

27817171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31797747-T-C

27818932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31798545-A-G

27819047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31798659-G-T

27819159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31798748-G-A

http://identifiers.org/hco/2/GRCh38#27819330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31798981-C-A

27819330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31798981-C-T

27819331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31798982-G-A

27819405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799083-T-A

27819405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799083-T-C

27819570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799351-A-G

27819576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799357-C-T

27819763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799534-T-C

http://identifiers.org/hco/2/GRCh38#27819810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31799579-C-A

27819814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799583-T-C

27820102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31799849-T-A

27820397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31800120-T-G

http://identifiers.org/hco/2/GRCh38#27822386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31801503-C-A

27822829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31801931-C-T

27822862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31801964-A-G

27823131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31802204-C-T

27823161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31802230-G-A

27825653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31803008-T-C

27826149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31803402-G-A

27826155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31803408-T-C

27826259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31803629-A-T

27827174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31804776-G-A

27827292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31804848-G-C

http://identifiers.org/hco/2/GRCh38#27827452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31804977-C-A

27827452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31804977-C-T

http://identifiers.org/hco/2/GRCh38#27827498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31805020-C-A

27827498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31805020-C-T

27827520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31805040-T-A

27827520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31805040-T-C

27827698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 31805196-A-G

http://identifiers.org/hco/2/GRCh38#27827846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31805342-C-A

27827846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31805342-C-G

27827899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31805395-A-G

27831005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31807639-T-C

27831310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31807882-T-C

27832072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31808346-C-T

27832202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31808540-T-C

27832419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31808896-A-G

27832480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31808964-A-G

27832516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31808998-G-C

27832550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809032-A-G

27832599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809072-T-C

27832624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809097-G-C

27832624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809097-G-T

27832637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809110-G-A

27832637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809110-G-T

27832680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809147-C-G

27832680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809147-C-T

27832798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809265-G-T

27832867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809382-G-T

27832916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809431-G-A

27832916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809431-G-C

27832916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809431-G-T

27832924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809439-T-G

27833030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809547-A-T

27833142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31809651-G-A

http://identifiers.org/hco/2/GRCh38#27833339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31809830-C-A

27833552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31810051-A-G

27833554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31810053-G-A

27833882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31810345-G-A

27834130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31810567-T-A

27834332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31810764-C-T

27834676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31811790-A-G

27834791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31811906-A-G

27834887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31812001-A-G

27834895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31812009-A-G

27835908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31812419-C-T

27838702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31812777-G-A

27838709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31812784-A-T

27839040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31813047-G-A

27839401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31813441-A-T

27841283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31814759-C-T

27841313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31814782-T-C

27841516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31815416-G-A

27841773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31815948-T-C

http://identifiers.org/hco/2/GRCh38#27842002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31816338-C-A

http://identifiers.org/hco/2/GRCh38#27842004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31816340-C-A

27842028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31816352-T-G

http://identifiers.org/hco/2/GRCh38#27843023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31817207-C-A

27843023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31817207-C-T

27843058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31817242-T-C

27843079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31817263-G-A

27843079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 31817263-G-C

27843247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31817431-A-G

http://identifiers.org/hco/2/GRCh38#27843312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31817479-C-A

27843312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31817479-C-T

27843559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818061-G-A

27843588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818090-G-A

27843588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818090-G-T

27843743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818253-A-G

27843743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818253-A-T

27843802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31818320-G-A

27844743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31819859-A-G

27844744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31819863-T-C

27845785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822104-G-A

http://identifiers.org/hco/2/GRCh38#27846379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31822423-C-A

27846511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822549-C-T

27846751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822823-C-G

27846828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822902-G-C

27846942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822974-G-C

27846942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31822974-G-T

27846984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31823004-T-A

27847010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31823030-T-C

27847583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31823593-G-T

http://identifiers.org/hco/2/GRCh38#27847633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31823643-A-C

27847914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31823897-T-C

27847932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31823915-C-T

http://identifiers.org/hco/2/GRCh38#27847952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31823935-C-A

27847996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31824169-G-A

27847996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31824169-G-T

27848027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31824198-A-G

27848100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31824271-G-A

27848100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31824271-G-C

27848100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31824271-G-T

27848132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31824303-A-G

27855546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31827481-A-T

27855699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31827611-G-A

27855805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31827709-A-G

27856219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31828515-C-G

27856219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31828515-C-T

27856233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31828528-T-C

27856373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31828659-A-G

27856397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31828690-A-T

27856860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829110-T-C

27856872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829122-G-A

27856907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829156-C-T

27856934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829183-T-C

27856946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829195-C-G

27856974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829221-A-G

27857408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829619-T-A

27857449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829643-C-T

http://identifiers.org/hco/2/GRCh38#27857460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31829653-C-A

27857498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829690-G-A

27857735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829901-T-C

http://identifiers.org/hco/2/GRCh38#27857751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31829917-C-A

27857790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31829956-T-C

27858065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830221-T-C

27858146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830293-T-G

27858288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830411-G-C

27858288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830411-G-T

http://identifiers.org/hco/2/GRCh38#27858333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31830553-C-A

27858333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830553-C-T

http://identifiers.org/hco/2/GRCh38#27858343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31830572-C-A

27858744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31830939-G-C

27859112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831252-G-A

27859213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831329-C-G

27859427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831505-C-T

27859438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831516-T-C

27859484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831562-G-T

http://identifiers.org/hco/2/GRCh38#27859647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31831684-C-A

27859700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831715-C-T

http://identifiers.org/hco/2/GRCh38#27859718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31831729-C-A

27859718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831729-C-T

27859725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831736-T-C

27859746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831757-T-A

27859772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831770-G-A

27859987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31831984-G-A

27860085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832080-C-G

27860576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832560-C-T

27860596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832579-A-G

27860603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832586-T-A

27860603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832586-T-C

27860612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31832594-G-A

27860827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833058-T-C

27860829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833060-C-T

27861037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833389-G-A

27861113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833454-G-A

http://identifiers.org/hco/2/GRCh38#27861198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31833620-C-A

27861248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833674-A-G

27861264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833690-A-G

http://identifiers.org/hco/2/GRCh38#27861345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31833752-A-C

27861345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31833752-A-G

27862774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31835984-G-A

27863017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31836824-G-A

27863017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31836824-G-T

27863290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31837071-T-C

27863359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31837138-T-G

27863578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31837357-T-C

27864452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31838751-A-G

27864500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31838793-A-G

27864631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31838905-C-G

http://identifiers.org/hco/2/GRCh38#27867446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31841530-A-C

27867464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31841548-G-A

27867464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31841548-G-C

27867756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31841897-G-A

27867906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31842038-T-C

27867906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31842038-T-G

27868333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31843079-G-C

27868622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31843325-T-C

27868634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31843337-C-T

27872536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31844732-C-T

27872784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31844891-C-T

27872823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31844930-C-T

27873822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31847012-G-A

27873822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31847012-G-T

27883575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31847979-G-A

27883703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31848039-T-C

http://identifiers.org/hco/2/GRCh38#27883812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31848152-C-A

27883812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31848152-C-T

27884667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31849055-C-T

27884669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31849057-G-C

27885077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31849436-G-A

27885091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31849450-C-G

27885346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31849710-T-C

27885811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31850154-C-G

http://identifiers.org/hco/2/GRCh38#27886051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31850467-C-A

27886051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31850467-C-T

27886772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851010-G-A

27886790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851028-T-A

27887121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851315-G-A

27887361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851511-G-T

27887485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851628-C-G

27887582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851697-A-G

27887851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851844-T-C

27887927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31851921-A-G

27889012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31853042-T-C

27889469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854142-A-G

27889487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854159-A-T

27889540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854207-G-A

27889540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854207-G-C

27889540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854207-G-T

27889687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854366-T-G

27889707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854408-T-C

27889785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854462-A-T

http://identifiers.org/hco/2/GRCh38#27889814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854491-A-C

http://identifiers.org/hco/2/GRCh38#27889899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854564-A-C

27889899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854564-A-G

27889990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854620-G-A

27889990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854620-G-T

27889992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854622-A-G

27890009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854634-T-C

http://identifiers.org/hco/2/GRCh38#27890034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854651-A-C

http://identifiers.org/hco/2/GRCh38#27890072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854695-C-A

27890072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854695-C-T

http://identifiers.org/hco/2/GRCh38#27890127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854746-C-A

27890127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854746-C-T

http://identifiers.org/hco/2/GRCh38#27890196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31854802-C-A

27890196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854802-C-T

27890325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 31854925-G-A

27890325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 31854925-G-C

27890335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 31854935-G-C

27890360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854953-G-A

27890360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31854953-G-T

http://identifiers.org/hco/2/GRCh38#27890430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31855022-C-A

http://identifiers.org/hco/2/GRCh38#27890440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31855032-C-A

27890440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855032-C-G

27890440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855032-C-T

27890441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855033-G-A

27890441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855033-G-C

27890441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855033-G-T

27890442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855034-G-A

27890462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855054-G-A

27890462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855054-G-C

27890462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855054-G-T

27890516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855108-T-C

27890516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855108-T-G

http://identifiers.org/hco/2/GRCh38#27890518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31855110-C-A

27890518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855110-C-G

http://identifiers.org/hco/2/GRCh38#27890582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#31855177-C-A

27890582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855177-C-T

27890597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855189-G-A

27890597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855189-G-C

27890597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30325
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31855189-G-T