44726336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93165386-A-G

44726390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93165360-A-G

44726441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93165311-G-T

44726581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165188-G-A

44726634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165129-A-G

44726697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165074-G-A

44726697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165074-G-T

44726748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165046-G-A

44726748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165046-G-T

44726796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165008-G-A

44726796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93165008-G-T

http://identifiers.org/hco/11/GRCh38#44726825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93164985-C-A

44726825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164985-C-T

44726833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164977-G-A

44726833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164977-G-T

http://identifiers.org/hco/11/GRCh38#44726850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93164953-A-C

44726850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164953-A-G

http://identifiers.org/hco/11/GRCh38#44726867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93164936-C-A

44726867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164936-C-T

44726894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93164908-G-C

44726993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164811-G-A

http://identifiers.org/hco/11/GRCh38#44727008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93164797-C-A

44727008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164797-C-T

44727161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164710-G-A

http://identifiers.org/hco/11/GRCh38#44727168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93164703-C-A

44727376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93164568-G-A

44727376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93164568-G-T

44727463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93164489-G-T

44727698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93164264-A-G

44727831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93164140-C-T

44727947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93164017-T-G

44728185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93163782-G-T

44728425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93163597-G-A

44728425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93163597-G-C

44728628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93163444-G-C

44728829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93163288-G-A

44728914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93163215-C-T

44729170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93162935-A-G

http://identifiers.org/hco/11/GRCh38#44729391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93162703-C-A

44729427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162669-T-G

44729450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162648-G-A

44729823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162309-T-A

44729856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162297-T-C

http://identifiers.org/hco/11/GRCh38#44729918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93162239-C-A

44729918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162239-C-T

44729960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162197-C-G

44729994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162175-G-A

44730162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93162024-G-C

44730603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161604-G-A

44730606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161602-G-A

44730678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161550-C-T

44731724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161039-G-T

44731728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93161035-C-T

44732025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160774-T-G

44732050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160754-C-T

44732200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160631-G-A

44732408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93160438-G-A

44732705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93160074-A-T

44733554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93159334-G-T

44733619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93159270-G-A

44733653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93159231-C-T

http://identifiers.org/hco/11/GRCh38#44734830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93158751-C-A

44734830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158751-C-T

44734831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158750-G-A

44734831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158750-G-C

44734831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93158750-G-T

44740127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157771-C-T

44740218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157680-G-A

44740247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157657-C-T

44740369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157532-C-G

44740369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157532-C-T

44740403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157498-G-A

44740421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93157480-G-C

44741275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93156690-A-G

44741278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93156687-C-G

44741784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93156191-T-G

44743505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155825-C-T

44743563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155767-C-T

44744000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155347-G-C

44744293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155036-G-A

44744302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155027-G-A

44744303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93155026-C-T

44744594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93154741-G-A

44744908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93154480-A-T

44744977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93154411-A-G

44745089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93154335-T-C

44750520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93153144-C-T

44750584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93153054-C-G

44750627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93152991-G-T

44750968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152666-T-C

44751108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152578-G-T

44751190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152500-A-G

44751319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152369-T-A

http://identifiers.org/hco/11/GRCh38#44751468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93152194-A-C

44751488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152174-A-G

44751538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152128-T-G

44751585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93152082-C-T

44752094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93151865-A-G

44753663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93150255-A-G

44753782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93150157-G-A

44754151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93149812-G-A

http://identifiers.org/hco/11/GRCh38#44754172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93149792-A-C

44754290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93149618-T-C

44754343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93149566-G-A

44754425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93149484-G-A

44754554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93149367-G-A

44755473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147865-C-T

http://identifiers.org/hco/11/GRCh38#44755667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93147671-C-A

44755667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147671-C-T

44755706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147633-A-G

44755845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147507-C-T

44756280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147226-C-G

44756381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93147145-T-C

http://identifiers.org/hco/11/GRCh38#44759514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93146425-C-A

44759597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93146358-C-G

44759978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145956-G-C

44760138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145789-T-C

44760230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145696-T-G

44760231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145695-G-A

44760466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145475-G-T

44760518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145412-A-G

44760834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145057-G-A

44760834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93145057-G-T

44760894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93145008-T-C

44761667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93144370-C-T

44761858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93144202-C-T

44761909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93144150-G-T

44762278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93143891-A-G

44762682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93143434-G-A

44762759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93143364-G-A

44762759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93143364-G-T

44762983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93143229-T-C

44763291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142963-T-C

44763362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142893-A-G

44763375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142880-G-C

44763594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142680-C-T

44764402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142393-T-C

44764642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142171-A-G

44764642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142171-A-T

44764704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93142110-G-A

http://identifiers.org/hco/11/GRCh38#44764839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93142039-A-C

44765030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141902-G-A

44765127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141835-G-A

44765655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141706-T-C

44765982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141308-T-C

44766122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141201-C-G

44766136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141187-T-C

44766198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93141124-T-C

44766715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93140837-A-G

44766717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93140835-A-G

44766959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93140691-C-T

44773901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134871-G-A

44773978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134789-C-T

44774318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134482-G-A

44774318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134482-G-T

44774375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134437-A-G

http://identifiers.org/hco/11/GRCh38#44774393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93134419-C-A

44774468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134343-G-A

44774483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134328-A-G

44774637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93134189-C-T

44774938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93133931-A-G

44774963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93133905-A-G

44774997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93133869-C-T

44775346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131940-G-A

44775519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131809-C-T

44775536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131792-T-C

44775536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131792-T-G

44775936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131230-T-C

44775967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93131199-T-C

44776211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93130974-G-A

44776349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93130841-C-T

44776966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93130154-G-T

44777016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93130115-T-G

44777562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93129369-T-C

44777562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93129369-T-G

44777697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93129242-C-T

44777814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93129134-C-G

44783329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93123786-G-A

44783329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93123786-G-C

44783375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93123747-T-C

44783479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93123686-A-T

44784631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122537-C-T

44784651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122519-C-G

http://identifiers.org/hco/11/GRCh38#44784741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93122430-C-A

44784754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122418-G-A

44784812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122369-C-T

44784830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122351-G-T

44784836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122345-G-A

44785028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93122145-C-T

44785503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121815-C-G

44785521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121806-C-T

44785532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121795-C-T

http://identifiers.org/hco/11/GRCh38#44785615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93121712-A-C

44785669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121658-C-G

http://identifiers.org/hco/11/GRCh38#44785682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93121650-C-A

44788021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121305-C-G

44788021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121305-C-T

44788144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121177-T-C

44788316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93121004-G-A

44789766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93120715-A-T

44789770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93120711-G-A

http://identifiers.org/hco/11/GRCh38#44793702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93118082-C-A

44794405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93117364-T-C

44794405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93117364-T-G

44794848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93117180-A-T

http://identifiers.org/hco/11/GRCh38#44795210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93116870-C-A

44795210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93116870-C-T

44795392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93116717-G-T

44796020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93116496-G-T

http://identifiers.org/hco/11/GRCh38#44796084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93116443-C-A

44796644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115933-T-C

44796975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115651-G-T

44796982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115644-C-G

44797044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115612-T-C

44797261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115422-G-C

44797339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115371-G-C

44797689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115150-T-C

44797899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93115052-G-A

44798037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93114932-T-C

44798501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93114565-G-A

44798743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93114331-G-A

http://identifiers.org/hco/11/GRCh38#44798985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93114093-A-C

44798985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93114093-A-T

44799088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93113983-G-T

44799136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93113938-G-A

44799415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93113652-A-G

44799587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93113417-C-T

44804794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93109117-A-G

44804794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93109117-A-T

44804866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93109025-A-G

44805535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93108408-G-A

44805595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93108353-T-G

44805849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93108106-A-G

44806662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93106704-C-T

44806731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93106644-C-G

44806861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93106557-G-A

44806866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93106552-G-T

44808123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93104951-T-A

44808128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93104946-C-G

44808131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93104943-G-A

44808180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93104895-G-A

44808271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93104806-G-A

44811180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93103539-G-C

44812901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93102085-G-A

44812996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93102011-C-G

44813032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93101976-G-T

44813046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93101963-G-A

44813080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93101933-A-G

http://identifiers.org/hco/11/GRCh38#44813436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93101588-C-A

44813560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93101255-C-T

44813951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93100866-A-T

44814570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93100551-G-A

44814570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93100551-G-C

44814658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93100464-C-G

44816996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93099741-G-A

44817086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93099676-T-C

44817423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93099354-G-A

44817458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93099330-C-T

44817531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93099284-G-A

44817730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93098982-A-G

44817744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93098959-C-T

44817767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93098898-C-G

44818014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93098590-A-G

44818451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93098160-C-T

44818823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93097833-G-C

44819174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93097546-G-C

44819611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93097103-C-T

44819666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93097048-C-T

http://identifiers.org/hco/11/GRCh38#44819943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93096783-A-C

44819943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096783-A-G

44819982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096753-C-G

44820288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096499-A-G

44820315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096478-C-T

44820470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096331-A-G

44820538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096272-C-T

44821117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93096112-C-T

44821384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93095863-A-G

http://identifiers.org/hco/11/GRCh38#44821490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93095739-A-C

44821655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93095568-T-C

44823865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092975-A-G

44824066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092809-C-T

44824092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092782-G-T

44824126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092748-T-A

44824130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092744-G-C

44824525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092439-G-C

44824752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092197-T-C

44824868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092078-T-A

44824900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93092040-C-T

44824974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93091983-A-G

http://identifiers.org/hco/11/GRCh38#44831470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93087856-C-A

44832167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087558-G-A

44832378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087379-A-G

44832378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087379-A-T

http://identifiers.org/hco/11/GRCh38#44832401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93087353-A-C

44832416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087338-C-T

44832601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087179-G-T

44832611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087170-C-T

http://identifiers.org/hco/11/GRCh38#44832752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93087054-C-A

44832783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93087030-G-A

44832813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086984-T-C

44833049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086778-C-G

http://identifiers.org/hco/11/GRCh38#44833099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93086736-C-A

44833099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086736-C-T

44833121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086713-T-C

44834101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086460-G-A

44834196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086390-G-A

44834196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086390-G-C

44834273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086320-G-A

44834292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086302-G-A

44834338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93086251-T-A

44835049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93085735-T-A

44835173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93085619-C-T

44835220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93085602-T-C

44839274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93084158-C-T

44839987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083599-C-T

44840040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083557-C-T

44840099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083506-C-T

44840155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083483-C-T

44840325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083311-T-C

44840456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93083180-T-G

44848253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93079551-C-T

44848278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93079537-G-A

44848278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93079537-G-T

44848356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93079468-G-T

44848397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93079437-G-C

44853837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078968-C-T

44854195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078637-G-A

44854195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078637-G-T

44854202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078627-G-T

44854251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078584-G-A

44854260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078575-G-C

44854309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93078531-C-T

http://identifiers.org/hco/11/GRCh38#44854896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93077917-A-C

http://identifiers.org/hco/11/GRCh38#44855601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93077202-A-C

44855611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93077193-C-G

44855698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93077142-C-G

44855785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93077079-T-A

44855785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93077079-T-C

44855822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93077053-T-C

44856279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076921-G-A

44856284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076916-C-G

44856434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076790-C-T

44856509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076716-C-T

http://identifiers.org/hco/11/GRCh38#44856693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93076560-C-A

44856693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076560-C-T

44856718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076535-T-C

44856835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076448-T-A

44856835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076448-T-C

44856835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076448-T-G

http://identifiers.org/hco/11/GRCh38#44856853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93076430-C-A

44856919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076352-C-G

44856919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076352-C-T

44857049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076229-G-A

44857053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076225-T-C

44857125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93076067-T-C

http://identifiers.org/hco/11/GRCh38#44857513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93075735-C-A

44857513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93075735-C-T

44857583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93075667-C-T

44858281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93075205-C-T

44858475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 93075151-A-G

44858856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93074804-T-C

44858919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93074742-G-T

44859209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93074448-G-A

44859209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93074448-G-T

44861999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073876-G-A

44862018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073867-C-T

44862036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073855-G-A

44862065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073830-G-T

44862143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073770-G-C

44862147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073766-G-T

44862262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073686-C-T

44862420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073467-G-T

44862442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073405-A-G

44862467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073328-T-C

44862504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93073288-C-G

44862884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93072946-C-T

44864309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93071290-T-G

44864314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93071285-A-G

44864545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93071071-C-T

44864812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93070876-A-T

44865317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93070425-T-C

44867920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068910-G-C

44867967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068866-G-A

http://identifiers.org/hco/11/GRCh38#44868102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93068700-A-C

44868186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068625-T-C

44868201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068610-C-G

44868221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068598-C-T

http://identifiers.org/hco/11/GRCh38#44868403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#93068372-C-A

44868403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068372-C-G

44868492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068044-G-A

44868492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068044-G-T

44868504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93068032-A-G

44868528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067944-C-T

44868648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067827-G-A

44868686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067792-A-G

44868692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067787-C-G

44868692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067787-C-T

44869129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93067357-T-C

44873192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93066514-C-T

44873234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93066480-G-A

44873272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93066445-T-G

44873295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93066428-C-G

44882113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93063212-G-T

44882261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93063043-C-G

44882383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93062945-C-T

44882627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93062767-C-G

44883315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93062125-G-A

44883337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93062121-G-T

44883367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93062099-G-A

44883475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93061998-C-T

44885154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93060976-C-T

44885187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93060949-G-C

44885223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93060909-C-T

44885376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93060769-A-G

44885495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron variant
orthologous variants: 93060621-C-T

44887344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059586-G-C

44887424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059504-T-C

44887586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059385-C-T

44887751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059225-G-C

44887751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059225-G-T

44887906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93059073-G-A

44892680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058871-G-A

44892729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058824-T-C

44892988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058620-G-A

44893002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058610-G-A

44893009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058603-C-T

44893092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058550-T-C

44893126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058520-G-A

44893167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058478-T-C

44893525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93058147-C-T

44893737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057965-T-C

44893920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057827-T-A

44893920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057827-T-C

44894073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057677-C-T

44894090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057660-G-A

44894159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057577-C-T

http://identifiers.org/hco/11/GRCh38#44894165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93057571-A-C

44894235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057496-G-A

44894622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057192-G-A

44894733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057081-C-T

44894793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93057022-C-T

44894842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056989-A-G

44894844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056987-T-C

44895206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056861-G-A

44895206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056861-G-T

http://identifiers.org/hco/11/GRCh38#44895424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93056651-A-C

http://identifiers.org/hco/11/GRCh38#44895563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93056554-A-C

44895572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056547-A-G

44895572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056547-A-T

44895606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056517-G-A

44895676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93056453-G-A

44896912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055858-G-C

44896989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055771-C-T

44896999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055761-G-T

44897246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055542-A-G

44897271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055514-G-C

44897286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055303-C-T

http://identifiers.org/hco/11/GRCh38#44897343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93055249-C-A

http://identifiers.org/hco/11/GRCh38#44897416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93055187-A-C

44897578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055061-T-G

44897620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055019-G-A

44897620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055019-G-T

44897637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055005-A-G

44897637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93055005-A-T

44897653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054993-T-C

44897661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054985-T-C

44897741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054926-T-C

44897808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93054860-G-A

44897848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054830-C-T

44897928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054780-G-T

http://identifiers.org/hco/11/GRCh38#44897940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93054767-C-A

44897940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054767-C-G

44897972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054720-T-G

44897973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054719-T-C

44898028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054666-A-G

44898056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054622-A-G

44898057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93054621-T-C

http://identifiers.org/hco/11/GRCh38#44898071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93054600-C-A

44906324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93053203-G-A

44906324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93053203-G-T

44906339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93053188-G-A

44906397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93053138-G-A

44906623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93052918-G-A

44906623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93052918-G-T

44906703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93052836-T-G

44907166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93052040-C-T

44908935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93051217-A-G

44909267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050962-G-A

http://identifiers.org/hco/11/GRCh38#44909379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93050876-C-A

44909379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050876-C-T

44909423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050832-G-T

44909434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050821-T-A

44909434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050821-T-C

44909466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050775-T-G

44909501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, undefined
orthologous variants: 93050739-A-T

44909529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050710-G-A

44909529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050710-G-C

44909529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050710-G-T

44909546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050696-T-C

http://identifiers.org/hco/11/GRCh38#44909613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93050638-C-A

44909613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050638-C-T

44909617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050634-G-A

44909629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050629-G-A

44909629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050629-G-T

44909633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050625-G-A

44909633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050625-G-T

44909636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050622-G-A

44909636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050622-G-T

44909682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050575-A-G

44909695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050568-G-A

44909695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050568-G-T

44909696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050567-C-T

44909726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050535-G-A

44909816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 93050445-C-T

44909870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050391-G-A

44909870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050391-G-C

44909870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93050391-G-T

44909942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050309-G-C

44909942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050309-G-T

44909943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050308-G-A

44909943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050308-G-T

44909952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050299-A-T

http://identifiers.org/hco/11/GRCh38#44909964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93050279-C-A

44909964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050279-C-T

44909970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050273-G-A

44910043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050190-A-G

44910044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050189-G-A

44910044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050189-G-C

44910044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050189-G-T

44910045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050188-A-G

44910045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050188-A-T

44910061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050146-C-G

44910061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050146-C-T

44910125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93050082-T-A

44910434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93049038-G-A

44910545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048949-C-T

44910546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048948-T-C

44910547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048947-T-C

44910646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048857-T-C

44910836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048336-G-A

http://identifiers.org/hco/11/GRCh38#44910857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93048314-A-C

44910955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048234-A-G

44911048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048154-C-T

44911193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93048034-G-A

44911248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93047988-T-C

44911615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93046427-C-T

44911830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93046209-C-G

44911830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93046209-C-T

http://identifiers.org/hco/11/GRCh38#44912432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93046034-C-A

44912579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045906-A-G

44912671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045818-A-G

44912673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045816-G-A

44912696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045791-G-A

44912786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045687-G-A

44912803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045662-G-T

44912821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045644-C-T

44913253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045172-A-G

44913266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045164-T-C

44913402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93045049-C-T

44913555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044944-A-G

44913625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044886-G-A

44913688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044848-G-A

44913688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044848-G-C

44914036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044600-A-G

44914036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044600-A-T

44914055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044575-G-A

44914099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044538-C-T

44914102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044535-G-T

44914217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044425-C-T

44914258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044344-G-C

44914271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044331-A-G

44914409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93044044-G-A

44915292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93043372-A-G

44916761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93043264-C-G

44916833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93043188-G-T

44917001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93043026-C-T

44917475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042690-G-T

44917488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042679-T-C

44917533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042607-G-T

44917550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042590-G-T

44917564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042577-G-T

44917567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042574-G-T

http://identifiers.org/hco/11/GRCh38#44917575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93042566-C-A

http://identifiers.org/hco/11/GRCh38#44917577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93042564-A-C

44917577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042564-A-G

44917697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042486-T-C

44917698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042485-G-A

44917698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042485-G-T

44917871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042310-T-C

44917947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042257-C-G

44918048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 93042159-T-G

44918104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042119-A-G

44918133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042094-G-A

44918133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042094-G-T

44918172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93042057-A-T

44918548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041714-G-T

44918549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041713-T-G

44918765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041616-G-A

44918777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041604-C-T

http://identifiers.org/hco/11/GRCh38#44918925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93041493-C-A

44918979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041440-G-A

44918979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041440-G-T

http://identifiers.org/hco/11/GRCh38#44919076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93041352-C-A

44919076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041352-C-G

44919162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041297-G-T

44919202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041277-C-G

44919268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93041211-G-A

44919333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041135-G-A

44919343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041125-T-C

44919343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041125-T-G

http://identifiers.org/hco/11/GRCh38#44919399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93041041-C-A

44919399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041041-C-G

http://identifiers.org/hco/11/GRCh38#44919418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93041028-C-A

44919418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041028-C-G

44919418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93041028-C-T

http://identifiers.org/hco/11/GRCh38#44919449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93040997-C-A

44919458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040988-A-G

44919597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040482-A-T

http://identifiers.org/hco/11/GRCh38#44919612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93040468-C-A

44919612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040468-C-T

http://identifiers.org/hco/11/GRCh38#44919639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93040442-C-A

44919640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040441-A-G

44919670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040415-C-T

44920064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040088-G-C

44920064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040088-G-T

44920133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040019-G-A

44920133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040019-G-T

http://identifiers.org/hco/11/GRCh38#44920139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93040013-C-A

44920139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040013-C-T

44920141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93040011-T-C

44920224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039956-G-A

44920649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039452-A-T

44920678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039403-T-C

44920826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039277-G-A

44920852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039251-C-T

44920919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039193-G-A

44920919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039193-G-T

44920993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93039124-A-G

44921170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93038985-G-T

44921284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93038846-G-A

http://identifiers.org/hco/11/GRCh38#44923185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93038044-C-A

44923270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037986-C-T

44923313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037943-G-A

http://identifiers.org/hco/11/GRCh38#44923408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93037910-A-C

44923408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037910-A-G

44923490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037862-T-G

44923569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037788-C-T

44923813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037565-C-T

44925415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037444-T-C

44925603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93037281-C-T

44926248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036526-G-A

44926248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036526-G-C

44926248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036526-G-T

http://identifiers.org/hco/11/GRCh38#44926261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036513-C-A

44926261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036513-C-T

44926298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036473-T-C

http://identifiers.org/hco/11/GRCh38#44926323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036446-C-A

44926323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036446-C-T

44926356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036399-A-G

44926367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036388-A-G

http://identifiers.org/hco/11/GRCh38#44926380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036378-A-C

http://identifiers.org/hco/11/GRCh38#44926419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036347-C-A

44926419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036347-C-T

44926463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036319-G-A

44926463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036319-G-T

http://identifiers.org/hco/11/GRCh38#44926495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036285-C-A

44926495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036285-C-G

44926495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036285-C-T

http://identifiers.org/hco/11/GRCh38#44926529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036268-C-A

44926529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036268-C-T

http://identifiers.org/hco/11/GRCh38#44926555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93036229-C-A

44926555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036229-C-T

44926601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036197-G-A

44926632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036167-T-C

44926641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 93036159-G-A

http://identifiers.org/hco/11/GRCh38#44926849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93035971-C-A

44926882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035956-G-A

44926882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035956-G-T

44926977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035891-G-A

http://identifiers.org/hco/11/GRCh38#44927082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93035823-A-C

44927095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035810-G-A

44927161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035763-G-A

44927161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035763-G-T

44927162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035762-G-A

44927162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035762-G-T

44927288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035690-A-G

44927555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035476-T-A

44927555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035476-T-C

44927558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035473-A-G

44927650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035396-C-T

44927725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035317-G-T

44928305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035277-A-G

http://identifiers.org/hco/11/GRCh38#44928332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93035250-A-C

44928410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93035172-A-G

http://identifiers.org/hco/11/GRCh38#44929052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034843-C-A

44929052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93034843-C-T

44929054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93034841-T-C

http://identifiers.org/hco/11/GRCh38#44929269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034648-C-A

44929269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034648-C-T

44929275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034642-G-A

44929275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034642-G-T

44929297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034620-A-G

44929297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034620-A-T

44929305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034612-G-A

44929305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034612-G-C

44929305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034612-G-T

http://identifiers.org/hco/11/GRCh38#44929337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034592-A-C

http://identifiers.org/hco/11/GRCh38#44929341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034588-A-C

44929341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034588-A-G

44929441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034489-A-G

44929441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034489-A-T

44929478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034452-G-A

http://identifiers.org/hco/11/GRCh38#44929500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034417-C-A

44929500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93034417-C-T

44929567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034372-G-A

44929695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034256-T-C

44929712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034242-G-A

http://identifiers.org/hco/11/GRCh38#44929830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034184-A-C

44929980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034105-T-C

http://identifiers.org/hco/11/GRCh38#44929988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034097-C-A

44929988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034097-C-T

http://identifiers.org/hco/11/GRCh38#44930127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93034015-C-A

44930127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93034015-C-T

44930527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033682-C-T

44930580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033591-G-A

http://identifiers.org/hco/11/GRCh38#44930602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93033569-C-A

44930602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033569-C-G

http://identifiers.org/hco/11/GRCh38#44930829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93033234-C-A

44930930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 93033180-T-G

44931025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033142-G-T

http://identifiers.org/hco/11/GRCh38#44931029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93033139-C-A

44931029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033139-C-T

44931048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033120-G-A

44931048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033120-G-T

44931101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033057-A-G

44931109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033044-G-T

44931113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93033040-T-C

44931172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032992-G-A

44931206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032960-G-A

44931206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032960-G-T

44931273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032895-G-A

44931273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032895-G-T

44931274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032894-C-T

44931284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032884-G-A

44931284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032884-G-C

44931284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032884-G-T

44931291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032877-G-T

http://identifiers.org/hco/11/GRCh38#44931373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93032819-C-A

44931430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032766-A-G

http://identifiers.org/hco/11/GRCh38#44931518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93032698-C-A

44931601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032620-G-T

http://identifiers.org/hco/11/GRCh38#44931722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#93032545-A-C

44931722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032545-A-G

44932063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032387-G-A

44932063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20660
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 93032387-G-T