http://identifiers.org/hco/6/GRCh38#10886850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41267646-A-C

10886864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267660-G-T

10886876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267672-T-C

10886876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267672-T-G

10886939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267716-A-G

10886998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267776-G-A

10886998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267776-G-C

10886998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267776-G-T

10887116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 41267884-G-A

10887116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 41267884-G-C

10887116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 41267884-G-T

10887124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267892-G-A

10887124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267892-G-C

10887124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 41267892-G-T

http://identifiers.org/hco/6/GRCh38#10887134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#41267902-C-A

10887134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 41267902-C-T

http://identifiers.org/hco/6/GRCh38#10887201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41267968-C-A

10887201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41267968-C-T

10887256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41268013-G-A

10887256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41268013-G-T

http://identifiers.org/hco/6/GRCh38#10887272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41268053-C-A

10887272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41268053-C-T

10887339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41268113-T-C

10887369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41268141-G-A

10891548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41269814-C-T

10891571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 41269834-A-G

10891586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269849-A-G

10891694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269888-A-G

10891694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269888-A-T

10891700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269894-G-A

10891700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269894-G-C

10891701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269895-T-A

10891708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269897-T-C

http://identifiers.org/hco/6/GRCh38#10891719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41269908-C-A

10891805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269977-T-C

10891814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41269986-A-G

http://identifiers.org/hco/6/GRCh38#10892039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41270207-A-C

http://identifiers.org/hco/6/GRCh38#10892064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41270232-A-C

10892064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41270232-A-G

10892136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41270296-C-T

http://identifiers.org/hco/6/GRCh38#10893883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41271503-C-A

10893883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 41271503-C-T

10893903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 41271523-G-A

10894006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 41271626-C-T

10894293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272163-G-A

10894311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272181-T-A

10894311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272181-T-G

10894340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272244-G-A

10894340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272244-G-T

http://identifiers.org/hco/6/GRCh38#10894344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41272248-C-A

10894344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272248-C-T

10894525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41272886-C-G

http://identifiers.org/hco/6/GRCh38#10894548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41272909-A-C

10894630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41273007-A-G

10894780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41273159-T-C

10894849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41273215-G-A

10894879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41273245-G-A

10894880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41273246-G-A

http://identifiers.org/hco/6/GRCh38#10895251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41274856-C-A

10897003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41275804-A-G

10897004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41275805-G-A

10897443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41276454-T-C

10897566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41276533-C-T

10897983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41276870-G-A

10898128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277015-T-A

10898152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277036-A-G

10898620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277293-A-G

10898653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277326-T-A

10898653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277326-T-G

10898762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277439-A-G

10898889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277558-A-G

10898904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277573-T-A

10898904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277573-T-C

10898911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277580-G-T

10898915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277582-A-G

10898916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41277583-A-G

http://identifiers.org/hco/6/GRCh38#10899673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41278828-C-A

10899835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41279378-A-G

10900053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41279574-A-T

10902728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 41282953-C-T

10905790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287235-C-G

10905885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287333-T-G

10905921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287358-A-G

10905921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287358-A-T

10905927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287364-A-G

10905927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287364-A-T

10905978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287388-G-T

10906013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41287423-G-T

10906099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287501-A-G

10906152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287554-A-G

10906170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287572-G-A

10906170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287572-G-T

10906198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287595-T-G

10906410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287792-T-C

10906415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287797-A-G

10906553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41287945-G-T

10906898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288158-C-G

10907491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288496-T-C

10907502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288507-G-A

10907507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288512-G-A

10907507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288512-G-T

10907522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288528-A-G

10907617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 41288623-A-G

10907631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 41288637-G-A

10907713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288711-A-G

10907755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288752-G-A

10907755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288752-G-T

10907772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288767-G-A

10907772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41288767-G-T

10908158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289133-A-G

10908211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289191-A-G

10908403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289382-G-C

10908451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289445-C-T

http://identifiers.org/hco/6/GRCh38#10908538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41289528-A-C

10908777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289745-G-T

10908779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41289747-A-G

10909043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41290685-T-C

10909456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41290779-C-T

10909530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41290853-G-A

10909591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41290920-C-T

10909615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41290944-G-A

10910225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41291448-T-A

10910225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41291448-T-G

10910519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41291859-T-C

10910767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292105-T-C

10910824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 41292143-G-C

10910882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292203-C-G

10910882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292203-C-T

10910888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292209-G-A

10910903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292237-G-T

http://identifiers.org/hco/6/GRCh38#10910972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41292387-C-A

10910972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292387-C-T

10910973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41292388-T-C

10911234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293040-C-T

10911266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293071-G-A

10911410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293320-A-G

10911491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293391-G-T

10911596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293482-T-C

10911721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293601-A-T

10911833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293714-T-C

10911874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293755-C-T

10911879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41293760-G-T

10912078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294649-A-G

10912161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294732-G-T

10912262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294818-A-G

10912287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294844-A-T

10912318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294876-A-G

10912393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41294959-A-G

10912468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295037-G-A

http://identifiers.org/hco/6/GRCh38#10912583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41295102-C-A

10912583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295102-C-T

10912596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295113-T-G

http://identifiers.org/hco/6/GRCh38#10912621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41295136-C-A

http://identifiers.org/hco/6/GRCh38#10912628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41295143-C-A

10912629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295144-A-G

10912629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295144-A-T

10912641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295154-T-C

http://identifiers.org/hco/6/GRCh38#10912714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41295225-C-A

10912714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41295225-C-T

10912773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41295284-T-C

10912789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295300-A-G

10912814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295323-T-C

10912827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295335-T-C

10912853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295367-T-C

http://identifiers.org/hco/6/GRCh38#10912940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41295457-A-C

10912940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295457-A-G

10912965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295473-A-G

10912988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41295496-C-T

10924065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296573-A-G

10924091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296585-A-G

10924121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296613-G-A

10924198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296677-C-T

10924348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296810-G-A

10924355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41296818-T-G

10924506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41296934-G-A

10924506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41296934-G-T

10924565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41296993-T-A

10924565-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41296993-T-G

10924572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41297000-A-G

10924644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41297072-G-A

10924809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41297541-C-T

10925442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41297802-G-T

10925453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41297813-C-T

10925459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41297824-T-C

http://identifiers.org/hco/6/GRCh38#10925768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41298092-C-A

10925797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41298121-A-G

10925810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41298147-T-A

10925810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41298147-T-C

10925835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41298166-C-G

10926162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299387-G-A

10926210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299420-G-A

10926210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299420-G-T

10926223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299432-A-G

http://identifiers.org/hco/6/GRCh38#10926264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41299465-C-A

10926406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41299569-G-A

10926544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299693-T-C

10926546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299695-G-A

10926558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299701-G-A

10926558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299701-G-C

10926558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299701-G-T

10926579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299722-T-A

10926579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299722-T-C

10927148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299935-G-T

10927189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41299975-A-G

10927247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41300038-A-G

10927272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41300063-T-C

10929218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41300880-T-G

10929235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41300897-T-C

10929242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41300904-C-T

10929296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41300962-G-A

10930072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41305801-T-A

10930111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41305839-T-A

10930111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41305839-T-C

http://identifiers.org/hco/6/GRCh38#10930133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41305860-C-A

10930133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41305860-C-T

http://identifiers.org/hco/6/GRCh38#10930175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41305900-C-A

10930187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41305912-G-T

http://identifiers.org/hco/6/GRCh38#10930285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41306044-C-A

10930324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41306114-C-T

10930394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41306187-T-C

10930507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41306303-T-C

10930528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306324-G-A

10930528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306324-G-T

10930529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306325-T-C

10930529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306325-T-G

10930568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306359-C-G

http://identifiers.org/hco/6/GRCh38#10930629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41306424-C-A

10930629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306424-C-T

10931315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306799-A-T

10931338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306820-T-A

10931338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306820-T-C

10931338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306820-T-G

10931339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306821-G-C

10931339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306821-G-T

10931359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306831-G-C

10931359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306831-G-T

10931366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41306842-G-T

10931616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307057-T-A

10931616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307057-T-C

10931985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307106-A-G

10931985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307106-A-T

10931990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307110-C-G

10931990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41307110-C-T

10933575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41308580-C-T

http://identifiers.org/hco/6/GRCh38#10935115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41309049-C-A

10935216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41309151-G-A

http://identifiers.org/hco/6/GRCh38#10942320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41316423-C-A

10942352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316443-T-C

10942362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316456-T-G

10942396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316491-A-G

10942396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316491-A-T

10942415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316512-G-T

10942436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316523-T-C

http://identifiers.org/hco/6/GRCh38#10942461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41316550-C-A

http://identifiers.org/hco/6/GRCh38#10942479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41316568-C-A

10942479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41316568-C-T

10942593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316674-A-G

http://identifiers.org/hco/6/GRCh38#10942611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41316692-C-A

10942611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316692-C-T

10942617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316699-C-T

10942781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316870-G-A

10942781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41316870-G-T

10954868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41323841-C-T

10954904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41323882-T-A

10954949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41323933-C-T

10955227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325031-T-C

http://identifiers.org/hco/6/GRCh38#10955229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41325033-C-A

10955229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325033-C-T

10955251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325055-G-A

10955268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325075-T-G

10955283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325090-A-G

10955289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325096-T-A

10955289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325096-T-C

http://identifiers.org/hco/6/GRCh38#10955319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41325123-C-A

10955319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325123-C-T

http://identifiers.org/hco/6/GRCh38#10955320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41325124-A-C

10955320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325124-A-T

http://identifiers.org/hco/6/GRCh38#10955340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41325145-A-C

10955340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325145-A-G

10955340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325145-A-T

10955362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325168-G-A

10955362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325168-G-T

10955365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325171-G-A

10955365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325171-G-C

10955365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325171-G-T

10955910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325866-C-T

10956014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325975-G-A

10956014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325975-G-C

10956014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325975-G-T

10956025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325986-G-A

10956025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41325986-G-T

10956140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41326121-A-T

10956212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 41326193-C-T

http://identifiers.org/hco/6/GRCh38#10956268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41326235-C-A

10956276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326243-T-C

10956301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326247-A-G

10957132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326423-T-C

10957908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326836-G-A

10957909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326837-T-A

10958022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41326958-T-A

10958659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327176-G-T

10958679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327196-A-G

http://identifiers.org/hco/6/GRCh38#10958692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41327209-C-A

10958692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327209-C-G

10958698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327217-G-T

10958731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327244-A-G

10958767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327279-T-C

10958817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41327330-A-T

10958869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 41327382-T-C

10958942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327435-A-T

http://identifiers.org/hco/6/GRCh38#10958973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41327462-C-A

10958973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327462-C-T

http://identifiers.org/hco/6/GRCh38#10958974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41327463-C-A

10958974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41327463-C-G

10962909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 41328598-A-G

10962948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41328636-T-C

10963275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41329889-G-T

http://identifiers.org/hco/6/GRCh38#10963301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41329915-C-A

10963301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41329915-C-T

10963356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41329959-C-T

10963420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330022-T-C

10963502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330092-G-A

10963502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330092-G-T

10963612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330200-C-G

10963714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330288-T-C

10963718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330292-T-C

10963744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330321-A-T

http://identifiers.org/hco/6/GRCh38#10963834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41330412-C-A

10963834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 41330412-C-T

http://identifiers.org/hco/6/GRCh38#10963916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41330470-C-A

10963916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330470-C-G

10963916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330470-C-T

http://identifiers.org/hco/6/GRCh38#10963924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41330478-C-A

10963924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330478-C-T

10963936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330486-G-A

10963936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41330486-G-T

http://identifiers.org/hco/6/GRCh38#10973869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41331577-A-C

10973869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41331577-A-G

10973911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41331618-G-A

10973911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41331618-G-T

10973953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41331659-C-T

http://identifiers.org/hco/6/GRCh38#10973982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41331695-C-A

10973982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41331695-C-T

10974106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41331800-G-A

10974106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41331800-G-T

10974107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41331801-C-T

10974161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41331858-G-T

10974176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41331867-A-G

http://identifiers.org/hco/6/GRCh38#10974305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41331981-A-C

10974330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332006-G-T

10974344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332018-G-T

10975537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332616-G-A

10975537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332616-G-T

10975553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332631-T-A

10975893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332968-A-G

10975913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41332990-T-C

10976087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333177-A-G

10976274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41333910-C-T

http://identifiers.org/hco/6/GRCh38#10976275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41333911-A-C

10976448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41334026-G-A

10976477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21537
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41334056-G-A