http://identifiers.org/hco/4/GRCh38#46993664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71815404-A-C

46993664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: 71815404-A-G

46993779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: 71815518-G-T

46993792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: 71815531-T-C

http://identifiers.org/hco/4/GRCh38#46993815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71815554-C-A

46993815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5 prime UTR variant
orthologous variants: 71815554-C-T

46993944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71815687-T-A

46994043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815789-G-A

46994043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815789-G-C

46994043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815789-G-T

46994049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815791-A-G

http://identifiers.org/hco/4/GRCh38#46994050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71815792-C-A

46994083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815835-G-C

46994083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815835-G-T

http://identifiers.org/hco/4/GRCh38#46994088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71815840-C-A

46994088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815840-C-T

46994093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815843-G-A

46994093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815843-G-T

46994133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815894-G-A

46994133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815894-G-T

46994149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815910-G-A

46994243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815999-T-C

46994243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71815999-T-G

http://identifiers.org/hco/4/GRCh38#46994324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71816069-A-C

46994386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71816129-G-A

46994386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 71816129-G-T

46994435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816265-G-T

46994445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816275-G-T

46994466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816301-G-T

http://identifiers.org/hco/4/GRCh38#46994514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71816349-C-A

46994514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816349-C-G

46994837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816662-G-T

46994902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816720-G-T

46995076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71816904-G-A

46995204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71817010-A-G

46998149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71818137-T-C

46998267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71818260-T-C

47000230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820309-T-C

47000316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820394-T-C

47000434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820532-T-A

47000442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820540-T-A

47000652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820760-A-G

47000689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820807-G-A

47000784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820892-T-C

47000817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71820913-G-T

47000922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821015-G-A

47000951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821045-A-G

47001046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821143-A-G

47001306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821488-C-G

47001309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821491-A-T

47001336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821541-G-A

47001336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71821541-G-T

47002096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71822241-T-C

47002310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71822619-T-G

47002454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71822762-C-T

47002595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71822912-T-G

http://identifiers.org/hco/4/GRCh38#47002688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71823059-C-A

http://identifiers.org/hco/4/GRCh38#47002801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71823146-C-A

47003490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71823801-T-C

47003544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71823854-G-T

47003685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71824004-C-T

47006083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825433-C-T

http://identifiers.org/hco/4/GRCh38#47006132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71825482-C-A

47006132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825482-C-T

47006142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825492-A-G

47006179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825531-T-C

47006356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825659-G-A

47006356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825659-G-C

47006503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825782-T-C

47006677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71825916-A-G

47006857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71826117-A-G

47010404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71836155-T-C

47010643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71836401-A-G

47010711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71836473-T-C

http://identifiers.org/hco/4/GRCh38#47011245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71836994-C-A

47011245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71836994-C-T

47011536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71837261-C-T

47011574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71837299-T-C

47011621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71837363-G-C

47015588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71843977-C-T

47015815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71844225-T-C

47016017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71844426-G-C

47016110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71844473-T-G

47016112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71844475-A-T

47017303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71845019-T-C

47017342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71845063-G-A

47017626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71845356-T-C

http://identifiers.org/hco/4/GRCh38#47017640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71845370-A-C

47017910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71846044-C-T

47017912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71846046-G-A

47024018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851007-G-C

47024202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851169-T-A

47024202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851169-T-G

47024207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851174-T-G

47024356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851321-T-C

47024440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851394-C-G

http://identifiers.org/hco/4/GRCh38#47025677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71851711-A-C

47025859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71851894-C-T

http://identifiers.org/hco/4/GRCh38#47025938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71851964-C-A

47030662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856368-G-A

47030880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856566-C-G

47030991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856677-T-C

47030998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856684-C-T

47031007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856691-G-A

47031081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856757-G-A

47031164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71856827-G-A

47031428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71857136-T-C

47031446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71857154-G-A

47031446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: intron variant
orthologous variants: 71857154-G-T

47031592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71857300-G-A

47031592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71857300-G-T

http://identifiers.org/hco/4/GRCh38#47031603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71857311-A-C

47031603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71857311-A-G

47031859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857575-T-A

47031859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857575-T-C

47031995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71857713-G-A

47031995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71857713-G-C

47031995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71857713-G-T

http://identifiers.org/hco/4/GRCh38#47032010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71857728-C-A

47032010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857728-C-T

47032033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857756-A-G

http://identifiers.org/hco/4/GRCh38#47032036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71857759-C-A

47032036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857759-C-T

47032159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71857893-C-T

http://identifiers.org/hco/4/GRCh38#47032307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858040-C-A

47032307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858040-C-G

47032307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858040-C-T

47032328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858061-A-G

47032351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858084-C-T

http://identifiers.org/hco/4/GRCh38#47032451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858182-C-A

47032451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71858182-C-G

47032451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71858182-C-T

47032517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858252-G-A

47032517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858252-G-T

47032528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858263-T-C

http://identifiers.org/hco/4/GRCh38#47032608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858343-C-A

47032608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71858343-C-T

47032734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858474-G-T

http://identifiers.org/hco/4/GRCh38#47032843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858585-C-A

47032843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858585-C-G

47032926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858666-T-A

47032926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858666-T-C

47032935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858674-G-A

47032935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858674-G-C

47032935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71858674-G-T

http://identifiers.org/hco/4/GRCh38#47032980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858715-C-A

47033138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858878-A-G

http://identifiers.org/hco/4/GRCh38#47033159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71858898-C-A

47033159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71858898-C-T

47033297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859111-C-G

47033363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859180-G-A

47033723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859516-G-T

47033848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859666-G-A

47033881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859698-A-G

47033916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859741-T-C

47034014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859845-A-G

47034014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859845-A-T

http://identifiers.org/hco/4/GRCh38#47034084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71859915-C-A

47034103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71859933-G-C

47034234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71860137-C-T

47034705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71860582-T-A

47034714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71860591-T-G

47034745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71860622-G-A

47034945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71860816-T-A

47035161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861028-T-A

47035189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861057-C-T

47035546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861539-A-G

47035676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861675-G-T

47035838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861809-A-G

47035998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861964-C-T

47036033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71861996-A-G

47036411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71862326-T-C

47037246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71862795-G-A

47037601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863100-G-C

47037652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863150-C-T

47037684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863182-C-T

47037807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863296-T-C

47038116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863847-A-T

47038182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863911-T-C

47038269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71863999-G-A

47038334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864064-A-T

47038581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864339-C-T

http://identifiers.org/hco/4/GRCh38#47038691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71864547-C-A

47038696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864552-G-C

47038817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864755-T-C

47038817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864755-T-G

http://identifiers.org/hco/4/GRCh38#47038991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71864943-A-C

47039047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71864996-A-G

47039073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865022-A-G

47039102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865044-T-C

47039136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865078-G-A

47039136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865078-G-T

http://identifiers.org/hco/4/GRCh38#47039137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71865079-C-A

47039350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865272-A-G

47039563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865642-T-C

47039567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865646-A-G

47039575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865654-T-C

47039830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865864-A-G

47039830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71865864-A-T

http://identifiers.org/hco/4/GRCh38#47040052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71866078-C-A

47040052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866078-C-T

http://identifiers.org/hco/4/GRCh38#47040156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71866165-A-C

47040162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866171-A-G

47040240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866198-A-G

47040280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866205-T-C

47040648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866481-G-A

47040677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866510-T-A

47040782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866630-G-T

47040805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866653-A-T

47041035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71866876-C-T

http://identifiers.org/hco/4/GRCh38#47041155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71866985-C-A

47041196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867026-T-C

47041259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867087-T-G

http://identifiers.org/hco/4/GRCh38#47041357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71867180-A-C

47041373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867196-T-C

47041787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867594-C-G

47041787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867594-C-T

47041950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867766-A-G

47042115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71867932-A-G

47042198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868018-G-A

47042425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868202-T-C

47042511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868236-A-G

47042759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868445-A-G

47042764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868450-A-G

http://identifiers.org/hco/4/GRCh38#47042951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71868616-C-A

47042951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868616-C-T

47042984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868648-T-C

47043011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71868675-T-C

http://identifiers.org/hco/4/GRCh38#47043059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71868723-C-A

47043168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71868839-A-G

http://identifiers.org/hco/4/GRCh38#47043257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71868930-C-A

47043257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71868930-C-T

47043445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869120-C-T

47043468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869143-G-T

47043487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869160-G-T

47043489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869162-G-A

http://identifiers.org/hco/4/GRCh38#47043507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71869180-C-A

47043796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869402-G-A

47043868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869474-T-C

47044197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869742-T-C

47044212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869757-T-C

47044255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71869803-T-C

47044674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71870735-A-G

47044681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71870742-T-C

47044920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871608-T-A

47044932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871616-C-T

47045006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871686-T-C

47045052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871730-G-C

47045216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871883-G-A

47045335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71871999-T-C

47045411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71872061-A-G

47045830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71872391-A-G

47047884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873073-G-A

47047963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873149-A-T

47048021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873208-T-G

47048179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873363-G-A

47048268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873452-T-A

47048688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873854-G-A

47048803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873965-C-T

47048843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873979-G-A

47048843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71873979-G-C

47048992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874103-T-G

47049038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874134-T-A

47049055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874151-T-A

47049055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874151-T-C

47049055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874151-T-G

47049123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874213-C-T

47049137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874226-T-G

47049412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874479-T-C

47049481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71874547-A-G

47050068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71875053-A-G

47050625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71875675-G-A

47050625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71875675-G-T

47051027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71876061-G-A

http://identifiers.org/hco/4/GRCh38#47051113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71876138-C-A

47051147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71876170-C-T

47051568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71876518-G-C

47052613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71877504-G-A

47052616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71877506-C-G

47052864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71877903-G-A

47052983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878074-G-A

47052983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878074-G-C

47052989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878080-T-C

47053001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878092-G-A

47053256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878362-G-A

47053256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71878362-G-T

47054272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879292-G-A

47054333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879352-G-A

47054613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879578-G-T

47054892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879597-G-A

47055033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879695-G-C

47055218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879888-G-A

47055219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71879889-G-T

47055468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71880176-G-A

http://identifiers.org/hco/4/GRCh38#47055490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71880198-C-A

47055813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71880541-T-G

47055900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71880615-G-A

47056185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71881283-G-A

47056403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71881536-T-A

http://identifiers.org/hco/4/GRCh38#47056723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71882587-C-A

47056723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71882587-C-T

47056759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71882622-A-G

47056759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71882622-A-T

47056820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71882675-T-C

47057383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71883271-G-C

47057804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71883718-A-G

47057976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71883936-C-G

47058021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71883979-T-C

47058074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884031-G-A

47058074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884031-G-C

47058087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884049-G-T

47058427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884390-C-T

47058597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884572-G-A

47058597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884572-G-T

47058664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884648-T-C

47058763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884729-C-T

47058799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884766-A-G

47058808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884775-C-T

47058846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884853-G-A

47058852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884859-G-T

47058934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884932-T-A

47058945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884944-G-A

47058967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71884970-G-T

47059216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885210-A-G

47059279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885273-G-A

47059279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885273-G-T

47059727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885547-C-T

47059868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885660-T-G

47059905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71885696-A-G

47060319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886270-C-T

47060368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886305-G-T

47060532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886456-G-A

47060624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886560-G-A

47060698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886635-A-G

47060741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71886682-T-A

http://identifiers.org/hco/4/GRCh38#47061081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71887028-A-C

47061129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887077-G-A

http://identifiers.org/hco/4/GRCh38#47061244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71887149-C-A

47061302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887198-A-T

47061582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887358-A-G

47062063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887850-G-A

47062064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887851-C-T

47062095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887882-C-T

47062096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71887883-G-A

47062275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888061-C-T

http://identifiers.org/hco/4/GRCh38#47062323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71888113-A-C

47062323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888113-A-T

47062355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888146-A-T

http://identifiers.org/hco/4/GRCh38#47062677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71888639-A-C

47062717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888800-A-G

47062770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888953-T-C

47062776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71888959-C-T

47062896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71889104-C-G

47063037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71889241-A-G

47063132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71889336-C-T

47063386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71889591-T-C

47064850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71890174-T-C

47064878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71890202-T-C

47064958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71890282-A-G

47065388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71890706-G-T

47065604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71890917-T-C

47069086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891524-C-T

47069125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891562-G-A

47069125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891562-G-C

47069329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891730-C-T

47069378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891782-G-A

47069378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891782-G-T

47069401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891804-T-C

47069423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891820-T-C

47069597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891977-G-A

47069597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71891977-G-C

47071322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71892921-C-T

47071400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71893023-A-G

http://identifiers.org/hco/4/GRCh38#47071749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71893452-C-A

47071749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71893452-C-T

47072153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71893849-T-C

47072230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71893929-G-A

47072741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894435-A-G

47072761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894456-G-A

47072761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894456-G-C

47072851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894538-T-C

47072851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894538-T-G

47072933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894621-T-C

http://identifiers.org/hco/4/GRCh38#47072985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71894672-A-C

47072985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71894672-A-G

47073089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71895572-T-G

47073093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71895576-T-C

47073243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71895734-T-C

http://identifiers.org/hco/4/GRCh38#47073257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71895748-C-A

47073300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71895791-A-G

47073346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71895836-T-A

47074606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71897159-T-C

http://identifiers.org/hco/4/GRCh38#47074697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71897250-A-C

47075412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71898238-T-A

47075482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71898308-G-A

47075917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71899372-A-T

47075945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71899400-T-C

http://identifiers.org/hco/4/GRCh38#47075948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71899403-A-C

http://identifiers.org/hco/4/GRCh38#47076267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71899687-C-A

47076428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71899882-G-T

http://identifiers.org/hco/4/GRCh38#47076621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71900096-C-A

47076625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71900100-C-G

47076631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71900106-G-A

47076857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71900258-G-C

47076925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71900341-C-G

47077316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71900820-G-A

47078613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71902553-C-T

47078800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71902724-T-A

47078858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71902783-G-A

47078858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71902783-G-C

47080397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71902935-G-A

47080643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903123-T-C

47080924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903289-T-C

47080985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903351-G-A

47081005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903376-C-T

47081212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903592-T-C

47081221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903602-A-G

47081232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903614-A-G

47081414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71903771-A-G

http://identifiers.org/hco/4/GRCh38#47081689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71904039-A-C

47081689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904039-A-G

47081747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904091-C-T

http://identifiers.org/hco/4/GRCh38#47081826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71904175-A-C

47081881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904225-T-C

47081998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904362-C-T

47082014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904367-C-T

47082242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904592-T-G

47082260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71904608-A-G

47082703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71905044-C-T

47082861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71905203-T-C

47082919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71905262-T-G

47083046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71905388-G-A

47083439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71905761-T-C

47083670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906066-T-C

47083787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906184-A-T

47083867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906262-T-G

47084361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906725-G-C

47084557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906916-C-T

47084627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71906961-A-G

http://identifiers.org/hco/4/GRCh38#47084727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71907043-C-A

http://identifiers.org/hco/4/GRCh38#47084728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71907044-A-C

47084761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71907067-G-T

47084801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71907107-C-T

47085174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71907483-A-G

47085545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71907839-T-C

http://identifiers.org/hco/4/GRCh38#47085551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71907845-C-A

47085551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71907845-C-T

47085816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71908120-G-A

47085816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71908120-G-T

http://identifiers.org/hco/4/GRCh38#47085899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71908195-C-A

47086002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71908324-T-C

47086098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71908428-C-T

47086729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71909719-G-A

47086876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71909862-T-G

47086911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71909897-G-A

47086911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71909897-G-T

47087134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910143-C-T

47087665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910495-A-G

47087721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910531-T-A

47087721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910531-T-C

47087764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910577-G-A

47087775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910590-T-G

47087886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910701-G-A

47087911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910726-C-T

47087931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71910749-G-A

47088526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71912466-T-C

47088639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71912576-A-G

47088640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71912577-T-C

47088926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71912781-C-T

47089180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71913129-G-A

47089471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71913412-A-G

47089471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71913412-A-T

47089478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71913419-T-A

47089695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71913666-T-A

47090096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71914045-T-G

47090535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71914470-T-C

47090688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71914598-A-G

http://identifiers.org/hco/4/GRCh38#47093024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71916377-A-C

47093024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71916377-A-G

47093027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71916380-T-C

47093441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917170-C-T

47093463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917201-C-T

47093471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917209-T-C

47093482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917220-A-G

47093563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917300-A-G

47093574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917314-C-G

47093574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917314-C-T

47093832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917563-C-T

47093914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917637-A-G

47093973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917705-G-T

47094059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71917773-A-T

47094915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71918107-G-A

47094988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71918181-C-T

47095267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71918455-C-T

http://identifiers.org/hco/4/GRCh38#47095288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71918476-A-C

47095653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71918811-A-G

47095668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71918826-T-C

47095901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71919043-A-G

47096019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71919152-G-A

http://identifiers.org/hco/4/GRCh38#47096055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71919187-C-A

47096055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71919187-C-G

47098356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923152-G-A

47098356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923152-G-T

47098448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923251-T-G

http://identifiers.org/hco/4/GRCh38#47098458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71923261-C-A

47098694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923639-T-C

47098822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923877-G-A

47098835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71923889-T-C

47099038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924054-T-C

47099137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924149-A-T

47099381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924380-T-C

http://identifiers.org/hco/4/GRCh38#47099523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71924511-C-A

47099687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924708-C-T

47099770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924801-T-C

47099770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924801-T-G

47099794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924824-T-C

47099794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924824-T-G

47099798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71924828-G-T

http://identifiers.org/hco/4/GRCh38#47099847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71924875-C-A

47100297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925337-G-A

47100348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925387-G-T

47100498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71925522-T-C

47101835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71926763-C-T

http://identifiers.org/hco/4/GRCh38#47101853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71926781-C-A

47101953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71926883-G-A

47105817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71929938-G-A

47106010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71930192-C-G

http://identifiers.org/hco/4/GRCh38#47106339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71930508-A-C

47106450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71930606-G-A

47106450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71930606-G-C

47106925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931104-G-C

47106926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931105-C-T

47106964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931146-T-C

47107052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931233-A-T

47107147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931285-A-G

http://identifiers.org/hco/4/GRCh38#47107186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71931326-A-C

47107186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931326-A-G

47107486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931586-T-C

47107521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931621-A-G

47107535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931631-A-G

47107669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931753-T-C

47107686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931770-T-C

47107697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931781-T-C

47107746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931832-A-T

47107846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71931930-A-T

47108337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71932398-T-C

47108629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71932972-T-G

47108730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933077-T-C

http://identifiers.org/hco/4/GRCh38#47108825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71933294-C-A

47108851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933318-C-T

47108913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933384-A-G

47108953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933421-C-G

47109337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933754-G-A

47109461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933866-A-G

47109473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71933876-G-A

http://identifiers.org/hco/4/GRCh38#47109578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71934045-C-A

47109578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934045-C-T

47109636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934103-C-T

47110035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934512-G-A

47110035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934512-G-C

47110065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934541-A-G

http://identifiers.org/hco/4/GRCh38#47110103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71934578-A-C

47110103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934578-A-T

47110121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934590-T-C

47110348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934789-A-G

47110356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934797-T-G

47110401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934842-T-C

47110590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71934988-A-G

47110948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71935324-G-A

47110948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71935324-G-T

47111924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71935939-G-A

http://identifiers.org/hco/4/GRCh38#47112432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71935994-C-A

47112439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936001-G-A

47112712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936270-G-C

47113073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936623-T-C

47113073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936623-T-G

47113299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936682-T-C

47113408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936697-T-A

47113503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936796-G-A

47113707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71936988-A-G

47113762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937042-A-G

47113955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937190-C-T

47114070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937281-G-A

47114130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937337-T-A

47114384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937579-T-C

47114479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71937674-C-T

47115969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71941406-A-G

47115969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71941406-A-T

http://identifiers.org/hco/4/GRCh38#47116300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71950026-A-C

47116576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950251-G-C

47116579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950254-T-A

47116579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950254-T-G

47116595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950270-T-C

47117127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950406-C-T

47117365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950578-T-A

47117365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950578-T-C

47117488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950640-A-G

47117506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950657-C-T

47117572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71950732-C-T

47117806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951083-C-T

47118142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951471-A-T

http://identifiers.org/hco/4/GRCh38#47118276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71951580-C-A

47118293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951597-T-C

47118468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951756-T-A

47118468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951756-T-C

47118581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71951863-C-T

47118784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71952065-G-T

47118842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71952123-T-G

http://identifiers.org/hco/4/GRCh38#47121760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71954387-A-C

47121772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71954399-G-A

47122028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71954622-A-G

47122458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955376-G-A

http://identifiers.org/hco/4/GRCh38#47122522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71955434-A-C

http://identifiers.org/hco/4/GRCh38#47122583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71955500-C-A

47122669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955574-G-A

47122675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955580-T-C

47122831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955724-A-G

47122933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955826-C-G

47122933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955826-C-T

47123039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71955913-A-G

47124127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71956233-G-T

47124359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71956454-G-A

47126141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71957609-A-G

47126167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71957628-T-G

47126513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71957957-C-T

47126529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71957974-A-G

47126647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71958105-T-C

47126687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71958137-A-G

47126913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71958352-G-T

http://identifiers.org/hco/4/GRCh38#47127031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71958474-C-A

47127046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71958489-A-G

47127235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71958673-G-A

47127591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960463-C-G

47127591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960463-C-T

47127716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960591-A-G

47127823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960676-A-G

47127836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960689-T-C

47127854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960707-A-T

47127967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960802-A-T

47128010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960833-G-A

47128015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960838-T-A

47128119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71960928-A-G

47128400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71961213-A-G

http://identifiers.org/hco/4/GRCh38#47128735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71961553-C-A

47131742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963004-T-C

47131877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963124-A-G

47132262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963484-T-C

47132470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963654-T-G

47132528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963701-G-T

47132651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71963810-C-T

47133001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71964121-T-C

47133181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71964300-C-T

http://identifiers.org/hco/4/GRCh38#47133987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71968246-A-C

47133995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71968254-T-A

47133995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71968254-T-C

http://identifiers.org/hco/4/GRCh38#47134130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71968385-C-A

47134327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71968586-A-G

47134431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71968683-C-T

47137575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71973836-T-C

47137665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71973929-A-G

47142913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71980154-G-A

47143236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71980425-G-A

47143262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71980461-A-G

47143358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71980561-C-T

47143616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71981255-C-G

47143630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71981287-T-C

47144632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985117-G-C

47144788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985282-A-G

47145028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985659-G-C

http://identifiers.org/hco/4/GRCh38#47145182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71985806-A-C

47145195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985819-G-T

47145270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985892-C-T

http://identifiers.org/hco/4/GRCh38#47145330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71985949-C-A

47145330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985949-C-T

47145360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71985978-A-G

47145806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71986539-T-C

47145887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 71986620-A-G

47146132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71986865-G-A

47146132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71986865-G-T

47146394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71987202-T-C

47147195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71987715-C-G

47147326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71987806-T-C

http://identifiers.org/hco/4/GRCh38#47147640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#71988066-C-A

47147941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71988329-T-A

47148196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71988542-G-A

47148256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71988576-T-C

47148395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71988690-C-T

47148944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71996977-T-C

47149127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71997155-G-A

47149203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71997232-A-G

47149282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71997286-A-G

47149545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71997543-T-C

47149578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71997576-A-G

47150065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 71999978-A-G

47150141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72000046-T-C

47150317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72000185-C-T

47150359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72000252-C-G

47150363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72000256-C-G

47150363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72000256-C-T

47150409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72000302-G-A

47150646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72000512-T-C

47150759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72000621-G-C

47152131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006345-G-T

47152279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006494-T-C

47152492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006697-A-G

47152536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006740-T-C

47152577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006776-G-A

47152627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006825-C-T

http://identifiers.org/hco/4/GRCh38#47152633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72006831-C-A

47152697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72006900-G-C

47153339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72016419-A-G

47153794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72016872-T-C

47153826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72016903-A-G

47153880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017111-G-C

47153999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017257-A-G

47154081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017354-G-C

47154114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017382-G-A

47154359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017607-G-C

47154359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017607-G-T

47154523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017784-G-A

47154676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72017913-G-A

http://identifiers.org/hco/4/GRCh38#47154803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72018010-A-C

47154936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018084-T-C

47155060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018196-G-A

47155134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018268-G-A

47155136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018270-T-C

47155319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018789-A-G

47155365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018834-A-G

47155565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72018981-G-A

47155646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72019062-A-T

47155657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72019073-C-G

47157021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72019554-A-G

47157250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72019784-G-A

47157255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72019789-G-A

http://identifiers.org/hco/4/GRCh38#47157495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72020023-A-C

47157775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72020294-T-C

47157925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72024830-G-A

47157979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72024884-T-C

47158489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72025431-G-A

47159642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72025595-G-T

47160120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026004-T-C

47160193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026057-C-T

http://identifiers.org/hco/4/GRCh38#47160403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72026257-C-A

47160403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026257-C-T

47160447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026301-A-G

47160492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026347-G-A

47161218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026719-T-C

47161368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 72026861-C-T

47161509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72026999-T-C

47162522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72028467-T-C

47162602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72028548-A-G

47162783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029193-C-T

47162808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029220-C-T

http://identifiers.org/hco/4/GRCh38#47162853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72029258-C-A

47162869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029273-C-T

47163213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029588-C-T

47163307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029682-T-C

47163320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029685-G-A

47163321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72029686-G-T

47164415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030106-A-T

47164469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030169-T-G

47164552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030251-G-A

47164634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030320-T-C

47164943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030556-G-A

47164943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030556-G-C

http://identifiers.org/hco/4/GRCh38#47165056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72030616-C-A

47165056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030616-C-T

47165161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030691-A-G

http://identifiers.org/hco/4/GRCh38#47165290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72030829-C-A

47165297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030836-C-T

47165298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030837-C-T

47165329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030866-C-T

47165420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72030953-C-T

http://identifiers.org/hco/4/GRCh38#47165852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72031303-A-C

47166020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72031460-T-C

47166042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72031482-C-T

47166051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72031491-A-G

47166151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72031642-C-T

47166989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72032024-T-C

47167346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72032378-A-G

http://identifiers.org/hco/4/GRCh38#47167944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72032808-A-C

47167978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72032817-C-T

47168125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72032928-T-C

47168600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033393-A-G

47168641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033427-T-A

47168641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033427-T-C

http://identifiers.org/hco/4/GRCh38#47168819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72033516-A-C

47168856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033551-T-C

http://identifiers.org/hco/4/GRCh38#47169043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72033723-C-A

47169124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033794-A-G

47169184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72033866-A-G

47169939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72038389-T-C

47170253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72038702-C-T

47170623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72039030-A-G

47170839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72039239-G-A

47171454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72039857-G-T

47171926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72042771-G-T

47172059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72042904-G-T

http://identifiers.org/hco/4/GRCh38#47172108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72042952-A-C

47172108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72042952-A-G

47172269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72043103-T-C

47172314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72043146-T-C

47172907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 72043451-G-C

47177313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72045894-T-G

47177534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046080-T-C

47177542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046088-A-G

47177579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046124-A-T

47177622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046164-A-G

47177624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046166-G-C

47177624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046166-G-T

47177662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046192-C-T

47177721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046252-C-T

47177838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046350-G-A

47177838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046350-G-T

47177843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046355-T-C

47177848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046360-G-T

47178325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046607-C-T

47178351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046631-G-C

47178351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046631-G-T

47178474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046754-G-A

47178519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046798-G-C

47178619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72046903-T-C

47178967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72047253-A-G

47179838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72049792-G-T

47181615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050317-G-A

47181615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050317-G-C

47181622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050325-G-A

47181622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050325-G-T

47181626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050329-A-G

47181633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050336-T-G

47181643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050346-A-T

47181703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050406-T-C

47181963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050667-T-G

47182037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050748-A-G

47182175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72050879-T-G

47183789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72052935-T-C

47183910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053055-T-C

47183937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053084-A-T

47184056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053279-A-G

47184247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053476-C-G

47184370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053581-T-C

47184405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053616-C-G

47184405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72053616-C-T

47184800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054391-T-A

47184841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054410-G-T

http://identifiers.org/hco/4/GRCh38#47184929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72054440-C-A

47184929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054440-C-T

http://identifiers.org/hco/4/GRCh38#47185029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72054502-C-A

47185029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054502-C-T

47185053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054525-C-T

47185085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054557-A-G

47185290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054747-T-A

http://identifiers.org/hco/4/GRCh38#47185338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72054795-A-C

47185338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72054795-A-G

http://identifiers.org/hco/4/GRCh38#47185540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72055381-C-A

47185580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055412-G-T

47185688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055509-C-T

47185732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055553-T-C

47185749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055570-T-A

47185749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055570-T-G

47185767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055587-T-C

47185842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055664-A-G

47186023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055845-T-C

47186088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72055918-A-G

47186165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057184-G-T

47186167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057186-A-G

http://identifiers.org/hco/4/GRCh38#47186206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72057239-C-A

http://identifiers.org/hco/4/GRCh38#47186207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72057240-A-C

47186207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057240-A-T

47186283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057339-A-G

47186402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057459-A-T

47186499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057553-A-G

47186505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057559-T-C

47186790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057764-G-A

47187005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057943-G-A

47187043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057981-A-T

47187058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72057996-T-G

47187215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72059959-A-T

47187270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72060012-A-G

47187656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72060744-C-G

47187656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72060744-C-T

47187823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72060885-T-C

47187823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72060885-T-G

47188076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061129-A-G

47188488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061463-G-A

47188488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061463-G-T

47188745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061709-T-A

47188821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061780-G-A

47188821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061780-G-T

47188930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72061885-T-C

47189267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72062093-A-T

47190427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72062564-G-T

47190864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72062978-T-C

http://identifiers.org/hco/4/GRCh38#47190952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72063049-A-C

47190952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72063049-A-G

47191297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72063427-C-T

47191396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72063824-T-A

47191405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72063844-C-T

47191550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72063998-A-G

47191582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064029-T-C

47191856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064340-G-A

47191856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064340-G-T

47191968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064446-T-G

47192011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064489-T-G

47192389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72064777-T-C

47193486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066089-T-A

47193557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066151-C-G

47193669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066262-T-A

47193760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066353-A-G

47193778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066381-G-A

47193778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066381-G-T

47193809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066411-T-G

http://identifiers.org/hco/4/GRCh38#47193920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72066516-C-A

47194020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72066612-G-C

http://identifiers.org/hco/4/GRCh38#47194724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72067490-C-A

47194759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72067526-T-G

47196253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72068109-T-C

47196673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72068330-G-T

47197065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72068742-G-A

47197211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72068870-T-C

http://identifiers.org/hco/4/GRCh38#47197739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72069357-C-A

47197739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069357-C-T

47197905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069511-T-C

47197974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069579-G-A

47198097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069698-G-C

47198302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069917-T-C

47198351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72069961-T-C

47200744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72071484-A-G

47200744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72071484-A-T

47200746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72071486-A-G

47200830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72071595-C-T

47200839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72071604-T-C

47201705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72072269-A-T

47201738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72072280-C-G

47201738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72072280-C-T

47202830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72073028-T-C

http://identifiers.org/hco/4/GRCh38#47203181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72073340-A-C

47203212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72073371-T-C

47203459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72073613-C-T

47203585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72074525-T-G

47203710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72074676-C-T

http://identifiers.org/hco/4/GRCh38#47204059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72075000-A-C

47204090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72075030-G-A

47204186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72075126-G-A

47204186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72075126-G-C

47204900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72075399-T-C

http://identifiers.org/hco/4/GRCh38#47205247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72075888-C-A

47205247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72075888-C-T

47205379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72076095-A-G

47205395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72076112-G-A

47205395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72076112-G-T

47205621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72076337-A-G

47205926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72076602-T-G

47206072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72077126-C-T

47206132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72077187-G-A

47206184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72077234-A-G

47206435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72077475-T-G

http://identifiers.org/hco/4/GRCh38#47206951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72078700-C-A

47206951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72078700-C-T

http://identifiers.org/hco/4/GRCh38#47207168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72078910-A-C

47207175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72078917-A-G

47207304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72079046-G-A

http://identifiers.org/hco/4/GRCh38#47207425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72079150-C-A

47207690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72079383-G-A

47207717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72079412-C-T

47208035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080312-A-G

47208069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080342-G-A

47208270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080555-A-G

47208270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080555-A-T

47208365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080650-G-A

47208365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080650-G-T

47208418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080696-A-G

47208480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080757-A-T

http://identifiers.org/hco/4/GRCh38#47208485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72080762-C-A

47208550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080805-T-A

47208550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080805-T-C

47208644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080879-A-G

47208690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72080948-G-A

47208780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081029-G-A

47208817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081065-A-G

47209021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081136-G-C

47209117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081177-T-C

47209433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081639-G-C

47209433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081639-G-T

47209438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72081644-T-C

47209828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72082763-T-C

47209890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72082812-C-T

47209967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72082879-G-A

47210033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72082943-G-T

47210112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72083023-T-A

47210130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72083041-G-C

47210262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72083163-T-G

47210282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083183-A-G

47210330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72083230-T-C

47210609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083475-A-G

47210672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083574-A-G

47210681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083582-A-T

47210722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083651-C-T

47210725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083654-T-G

47210765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083702-A-G

47210765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083702-A-T

47210771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72083708-T-C

47211153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72084083-A-T

47211176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72084106-G-C

47211399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72084324-T-C

47211493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72084430-G-T

47214066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 72087614-T-A

47215555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72087226-C-T

47215571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72087242-A-T

47215737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72087373-G-A

47216253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72087892-A-T

47216403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72089405-A-G

47216466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72089468-C-T

47216477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72089479-C-T

47216686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72089679-C-T

47216869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72089848-A-G

47217327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72090355-G-A

47219821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72092994-C-T

47219872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72093051-G-A

47220682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72093798-T-C

http://identifiers.org/hco/4/GRCh38#47220833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72093945-C-A

47220958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72094056-T-C

http://identifiers.org/hco/4/GRCh38#47221035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72094191-C-A

47221035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72094191-C-T

47222593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72095775-G-C

47222709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72095889-G-A

47222919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096094-T-C

47222927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096102-T-C

47223113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096299-C-T

47223134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096320-T-A

47223134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096320-T-C

47223136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096335-T-A

47223199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096398-T-A

47223249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72096455-T-C

47223649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72097073-T-G

47223650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72097074-G-A

http://identifiers.org/hco/4/GRCh38#47223690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72097114-A-C

47223690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72097114-A-G

47224071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72097440-A-G

47225250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72098963-G-C

http://identifiers.org/hco/4/GRCh38#47225251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72098964-A-C

47225296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72099010-T-G

47225619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72099293-T-C

http://identifiers.org/hco/4/GRCh38#47226021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72099662-A-C

47226198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72099823-T-C

47226772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72099949-T-G

47226797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72099975-T-C

47226993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72100176-G-A

47227029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72100202-A-G

47227264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72100403-A-G

http://identifiers.org/hco/4/GRCh38#47228067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72101091-A-C

47228215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72101220-C-G

47228220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72101224-T-C

47228515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72101538-G-A

47228657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72101684-C-T

http://identifiers.org/hco/4/GRCh38#47231398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72107614-A-C

47231426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107642-G-C

47231426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107642-G-T

47231432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107648-G-A

47231466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107681-G-T

47231693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107909-T-C

47231784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72107999-G-A

47233677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72109291-T-A

47233705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72109307-T-C

47234835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72110199-C-T

47234983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72110324-T-G

47239170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72111788-G-A

47239259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72111875-G-C

47239528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72112293-C-G

47239890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72112644-G-A

47239890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72112644-G-C

47239890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72112644-G-T

47240201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72112977-A-T

47240323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113107-T-C

47240708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113482-G-A

47240708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113482-G-T

47240754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113507-G-A

47240871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113613-A-T

http://identifiers.org/hco/4/GRCh38#47240915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72113657-C-A

47240958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72113700-T-G

http://identifiers.org/hco/4/GRCh38#47240976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72113718-C-A

47241357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72114046-T-A

47241582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72114276-A-T

47245261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72114510-A-G

http://identifiers.org/hco/4/GRCh38#47245534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#72114740-A-C

47245614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72114813-T-C

47253097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4081
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 72115308-A-G