138831764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100473-G-C

138831764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100473-G-T

138831854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100574-G-A

138831856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100576-G-A

http://identifiers.org/hco/7/GRCh38#138831898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38100617-C-A

138832014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100729-C-T

138832094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100798-C-T

138832534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100819-T-C

138832617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38100922-A-T

138832986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101295-A-G

138833083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101373-T-C

138833084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101374-G-A

138833084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101374-G-T

138833156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101429-C-G

138833156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101429-C-T

138833184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101457-A-G

138833499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101734-C-T

138833570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101806-C-T

138833594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101832-G-A

138833594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101832-G-T

138833622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101862-G-A

138833698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101903-C-T

138833715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101916-G-C

138833716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101917-G-T

138833745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101944-A-G

http://identifiers.org/hco/7/GRCh38#138833757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38101971-C-A

138833757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38101971-C-T

138833819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102035-T-C

138833848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102064-G-A

138833858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102074-T-C

138833858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102074-T-G

138833862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102078-G-A

138833862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102078-G-T

138833981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102139-A-G

138833981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102139-A-T

138834012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102166-A-G

http://identifiers.org/hco/7/GRCh38#138834035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38102189-C-A

138834035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102189-C-T

http://identifiers.org/hco/7/GRCh38#138834094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38102236-C-A

138834466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102316-T-C

138834486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102336-T-C

138834486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102336-T-G

138834549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102405-G-A

138834549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102405-G-T

138834636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102501-T-C

138834674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102542-G-A

138834814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102680-T-C

138834854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102720-T-C

138834875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102741-G-T

138835010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102875-T-A

138835134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38102982-A-G

http://identifiers.org/hco/7/GRCh38#138835140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38102988-C-A

138835161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103009-T-C

138835178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103026-G-T

http://identifiers.org/hco/7/GRCh38#138835199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38103045-C-A

138835199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103045-C-T

138835311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103150-T-C

138835393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103211-G-T

http://identifiers.org/hco/7/GRCh38#138835594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38103395-C-A

138835628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103422-G-A

138835653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103446-G-A

138835718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103484-T-A

138835718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103484-T-C

138835726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103492-T-C

138835927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103636-G-T

138836002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103670-G-A

http://identifiers.org/hco/7/GRCh38#138836501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38103846-C-A

138836501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103846-C-T

138836641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103957-T-C

138836641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38103957-T-G

138836751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104052-A-G

138836890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104183-T-A

138836910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104203-T-C

138836929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104224-A-G

138836957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104247-T-C

138837020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104308-C-T

http://identifiers.org/hco/7/GRCh38#138837039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38104322-C-A

138837039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104322-C-T

138837047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104330-A-T

138837067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104350-T-C

138837338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104632-T-C

138837639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104927-G-A

138837639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104927-G-T

138837650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104938-G-T

138837657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38104990-G-A

138837772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105121-G-A

138837772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105121-G-T

138837830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38105181-A-G

138837963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38105313-G-A

138837963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38105313-G-T

138838086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 38105436-G-A

138838086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 38105436-G-C

138838086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 38105436-G-T

138838149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38105499-G-A

138838171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105521-T-A

138838171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105521-T-C

138838196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105547-G-A

138838247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105579-G-T

http://identifiers.org/hco/7/GRCh38#138838267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38105600-C-A

138838295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105629-G-A

138838295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38105629-G-T

http://identifiers.org/hco/7/GRCh38#138838630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38106073-A-C

138839461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38107484-C-G

138839461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38107484-C-T

138839558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38107559-C-T

138840196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38107780-G-A

138840196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38107780-G-C

138840196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38107780-G-T

138840205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38107789-T-C

138840207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38107791-G-A

http://identifiers.org/hco/7/GRCh38#138840223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38107807-C-A

138840298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38107882-G-T

http://identifiers.org/hco/7/GRCh38#138840303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38107887-C-A

138840303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38107887-C-G

http://identifiers.org/hco/7/GRCh38#138843584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38111258-A-C

http://identifiers.org/hco/7/GRCh38#138843764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38112589-A-C

138843764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38112589-A-G

http://identifiers.org/hco/7/GRCh38#138844285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38113737-C-A

138844383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38113835-C-T

http://identifiers.org/hco/7/GRCh38#138844515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38113968-C-A

138844552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38114001-T-C

http://identifiers.org/hco/7/GRCh38#138844621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38114057-C-A

138844621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38114057-C-T

138852237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38116372-C-G

138852237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38116372-C-T

138852328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38116463-A-G

138860739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119201-A-G

138860955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119342-C-T

http://identifiers.org/hco/7/GRCh38#138861011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38119400-C-A

138861026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119415-T-C

http://identifiers.org/hco/7/GRCh38#138861044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38119433-A-C

138861075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119463-G-T

138861098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119486-A-G

138861113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119501-G-A

138861131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38119519-G-A

138861131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38119519-G-C

138861131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38119519-G-T

http://identifiers.org/hco/7/GRCh38#138861264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38119652-C-A

138861264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38119652-C-T

138861266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38119654-G-A

138861307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38119695-G-A

138861307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38119695-G-T

138861322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38119710-G-A

138861322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38119710-G-C

138861367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38119755-G-A

http://identifiers.org/hco/7/GRCh38#138861489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38119874-C-A

138861489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119874-C-T

138861512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38119936-A-G

http://identifiers.org/hco/7/GRCh38#138862921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38120296-A-C

138865635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38122262-G-A

138866204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38122864-A-G

http://identifiers.org/hco/7/GRCh38#138866216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38122876-A-C

138866314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38122968-C-G

138866366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123021-T-C

138866366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123021-T-G

138866387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123041-G-A

138866442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123082-G-A

138866492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123137-T-C

138866630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123227-G-A

138866702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123296-A-G

138867576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123759-T-A

138867759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123882-C-T

138867812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123922-C-T

http://identifiers.org/hco/7/GRCh38#138867835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38123944-C-A

138867835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123944-C-G

138867897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123983-G-A

138867897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123983-G-C

138867897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38123983-G-T

http://identifiers.org/hco/7/GRCh38#138867938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38124022-C-A

138867938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124022-C-T

138868008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38124088-G-A

138868047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38124127-G-A

138868050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38124130-C-T

138868246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124272-A-G

138868246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124272-A-T

138868248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124274-G-A

138868248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124274-G-T

138868261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124284-T-C

138868261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124284-T-G

138868266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124289-G-A

138868266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124289-G-C

138868266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124289-G-T

http://identifiers.org/hco/7/GRCh38#138868276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38124301-C-A

138868276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124301-C-G

138869093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124910-G-A

138869121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124936-G-A

138869121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38124936-G-C

138869311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125066-G-A

138869382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125145-G-C

138869480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125228-G-A

138869480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125228-G-T

138869514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125250-G-A

138869514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125250-G-T

138869651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38125384-G-A

http://identifiers.org/hco/7/GRCh38#138869669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38125402-C-A

138869669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38125402-C-G

138869669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38125402-C-T

138869702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38125435-C-T

138869782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125514-G-C

138869782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38125514-G-T

http://identifiers.org/hco/7/GRCh38#138870965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126328-C-A

138870969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126332-C-T

http://identifiers.org/hco/7/GRCh38#138870973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126336-A-C

138871064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126419-G-A

138871064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126419-G-T

http://identifiers.org/hco/7/GRCh38#138871116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126451-C-A

138871116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126451-C-T

138871193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38126527-G-A

138871193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38126527-G-T

138871205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous_variant, undefined
orthologous variants: 38126539-G-A

138871223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous_variant, undefined
orthologous variants: 38126557-C-G

138871223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous_variant, undefined
orthologous variants: 38126557-C-T

138871304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous_variant, undefined
orthologous variants: 38126638-G-A

http://identifiers.org/hco/7/GRCh38#138871342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126676-C-A

138871342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38126676-C-T

138871355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38126689-T-C

http://identifiers.org/hco/7/GRCh38#138871394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126725-C-A

138871394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126725-C-G

138871394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126725-C-T

138871435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38126766-T-A

138871438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126769-T-C

138871438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126769-T-G

138871458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126789-T-C

http://identifiers.org/hco/7/GRCh38#138871470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38126801-C-A

138871561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126865-C-T

138871562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38126866-A-G

138873158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38127489-C-G

138873171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38127502-T-G

138873278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38127605-T-C

138873278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38127605-T-G

138874298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38128317-C-T

138876816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38129933-C-G

138876883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38130002-C-G

138876973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38130085-T-A

138878278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38130586-C-T

138878482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38130901-C-T

138878960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38131525-G-A

138879001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38131585-C-T

138879376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38131927-G-A

138879475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132023-G-A

138879475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132023-G-T

138879487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132035-G-A

138879487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132035-G-T

138879575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38132102-G-A

138879575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38132102-G-T

138879597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38132124-G-A

138879597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38132124-G-C

138879597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38132124-G-T

138879716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132232-A-G

http://identifiers.org/hco/7/GRCh38#138879745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38132259-A-C

138879745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132259-A-G

138879825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132296-T-C

138879870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132342-A-G

138880035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132815-G-A

138880074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132851-T-C

138880079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132856-C-T

138880111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38132894-C-T

138880384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38133639-T-C

http://identifiers.org/hco/7/GRCh38#138880397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38133652-C-A

138880409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38133664-T-A

138880516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38133752-A-G

138880552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38133795-T-G

http://identifiers.org/hco/7/GRCh38#138880622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38133863-A-C

138880781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38133999-G-A

138881220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134818-C-T

138881266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134864-G-C

138881266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134864-G-T

138881285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134883-C-T

138881289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134887-G-A

138881289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134887-G-T

138881304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134902-A-T

http://identifiers.org/hco/7/GRCh38#138881306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38134904-C-A

138881306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38134904-C-T

http://identifiers.org/hco/7/GRCh38#138881307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38134905-C-A

138881416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38135011-G-C

138881429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38135024-G-C

138881476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38135071-G-A

138881489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38135084-T-A

138881513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38135108-T-A

138881513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38135108-T-C

138881519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38135114-G-A

138881607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135328-C-T

138881608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135329-A-G

138881615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135336-T-C

138881644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135429-A-G

138882065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135791-G-A

138882088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135812-C-T

138882167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135882-A-G

138882168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135883-C-T

138882210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135911-A-G

http://identifiers.org/hco/7/GRCh38#138882252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38135950-A-C

138882252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38135950-A-G

138882305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136054-T-C

138882346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136152-C-T

http://identifiers.org/hco/7/GRCh38#138882689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38136437-A-C

138882714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136461-T-C

138882714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136461-T-G

138882815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136529-C-T

138882888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136600-C-T

138883756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136802-G-A

138883756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38136802-G-C

138886232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38137152-T-C

138886270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38137185-G-A

138886835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38137432-C-G

138888626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38138690-G-T

138888632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38138696-A-G

138888871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38138998-T-C

138888897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139024-G-A

138889013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139146-C-T

138889019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139152-A-G

138889032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139164-T-C

138889323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139444-C-T

138889402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139519-G-A

138889415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139532-T-C

138889524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139645-G-T

138889577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139699-C-T

138889730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139827-C-G

138889795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139889-A-G

138889896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38139978-A-G

138890231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38140317-G-A

138890482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38140578-A-G

138890493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38140589-C-T

http://identifiers.org/hco/7/GRCh38#138890635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38140709-C-A

http://identifiers.org/hco/7/GRCh38#138890756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38140788-A-C

http://identifiers.org/hco/7/GRCh38#138890879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38140901-A-C

138890879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38140901-A-T

138891177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38141985-T-C

138891178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38141986-G-A

138891178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38141986-G-T

138891265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142059-G-A

138891265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142059-G-C

138891575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142357-A-G

138891709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142486-T-C

138891735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142513-A-G

138891735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142513-A-T

138891785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142557-G-T

138891826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142594-G-A

138891979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142722-T-C

138892090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142817-G-A

http://identifiers.org/hco/7/GRCh38#138892129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38142851-C-A

138892217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142940-A-G

138892246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38142960-G-C

138892720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38143382-G-A

138892747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38143417-A-G

138892877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38143918-T-C

http://identifiers.org/hco/7/GRCh38#138893057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38144077-C-A

http://identifiers.org/hco/7/GRCh38#138893121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38144144-C-A

138893302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144256-T-C

138893302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144256-T-G

138893315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144270-G-A

138893332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144287-G-A

http://identifiers.org/hco/7/GRCh38#138893470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38144377-C-A

138893470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144377-C-T

138893557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144463-G-A

138893619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144517-A-G

138894046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144757-G-T

138894215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38144920-A-T

138894316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145009-C-T

138894318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145011-C-G

138894318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145011-C-T

138894324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145017-G-A

138894423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38145107-G-A

138894462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38145146-G-A

138894484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38145168-T-C

138894498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38145182-C-G

138894498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38145182-C-T

138894538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145227-G-A

138894546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145235-G-A

138894561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145250-C-T

http://identifiers.org/hco/7/GRCh38#138894569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38145258-C-A

138894569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145258-C-T

138894598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145287-T-C

138894598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145287-T-G

http://identifiers.org/hco/7/GRCh38#138894616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38145305-C-A

138894616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145305-C-T

138894733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145378-C-T

138894734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145379-G-A

138894746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145389-T-C

138894789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145414-T-C

138894965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145558-C-T

138895158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145734-G-A

http://identifiers.org/hco/7/GRCh38#138895162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38145738-A-C

138895175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145751-G-A

138895249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145823-C-G

138895314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145887-G-A

138895335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145908-G-A

138895345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38145918-T-C

138896545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38147744-G-A

138897063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38147909-C-T

138897427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38148856-T-C

138897991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150198-T-C

http://identifiers.org/hco/7/GRCh38#138898334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38150224-C-A

138898455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150326-T-C

138898572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150445-T-G

138898593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150466-T-C

138898727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150603-C-T

138898785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150658-T-C

138898851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150895-A-T

138898852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150896-T-A

138898852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150896-T-C

http://identifiers.org/hco/7/GRCh38#138898855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38150899-A-C

138898855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150899-A-G

138898866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150910-T-A

138898867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150911-G-A

138898867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150911-G-T

138898877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38150946-C-T

138898902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151026-G-C

138898902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151026-G-T

138898910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151034-T-C

138898912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151036-C-T

http://identifiers.org/hco/7/GRCh38#138898913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38151038-C-A

138898913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151038-C-T

138898968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38151096-A-G

138899025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38151153-C-T

http://identifiers.org/hco/7/GRCh38#138899075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38151203-C-A

138899075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38151203-C-G

138899075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38151203-C-T

138899144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151272-C-T

138899201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151333-G-T

138899213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151344-T-C

138899250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151381-C-G

http://identifiers.org/hco/7/GRCh38#138899262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38151393-C-A

138899296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151425-A-G

138899296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151425-A-T

138899309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151437-C-G

138899309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151437-C-T

138899627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38151683-G-A

138901308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38152562-T-C

138901676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38152809-T-C

138901976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153288-C-T

http://identifiers.org/hco/7/GRCh38#138901985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38153301-A-C

138901985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153301-A-G

138902084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153387-T-C

138902295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153817-G-A

138902321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153835-T-C

138902338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153855-T-C

138902406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153887-C-T

138902426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38153907-T-C

138902558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154035-G-C

138902606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154083-G-C

138903302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154313-T-C

138903325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154336-A-G

138903394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154397-G-A

http://identifiers.org/hco/7/GRCh38#138903453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38154446-C-A

138903453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154446-C-T

138903462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154455-T-A

138903505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154484-G-A

138903505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154484-G-T

http://identifiers.org/hco/7/GRCh38#138903633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38154587-C-A

138903633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38154587-C-T

138903690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38154644-T-C

138903774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154726-A-G

138903774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154726-A-T

138903814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154761-T-C

138903947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154820-G-C

http://identifiers.org/hco/7/GRCh38#138904041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38154876-C-A

http://identifiers.org/hco/7/GRCh38#138904063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38154897-C-A

138904070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38154904-C-T

http://identifiers.org/hco/7/GRCh38#138904084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38154917-C-A

138904473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155259-G-A

138904595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155374-T-A

138904595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155374-T-C

http://identifiers.org/hco/7/GRCh38#138904622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38155399-A-C

138904644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155424-T-A

138904644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155424-T-C

http://identifiers.org/hco/7/GRCh38#138904693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38155460-C-A

http://identifiers.org/hco/7/GRCh38#138904694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38155461-A-C

138904804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155553-G-A

138904875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155620-G-T

http://identifiers.org/hco/7/GRCh38#138904947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38155693-C-A

138904947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155693-C-T

http://identifiers.org/hco/7/GRCh38#138905007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38155751-A-C

138905007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155751-A-G

138905106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155848-A-G

138905155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38155928-A-G

138905285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38156045-G-A

138905400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38156155-G-A

http://identifiers.org/hco/7/GRCh38#138905433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38156187-C-A

138905501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38156260-A-G

http://identifiers.org/hco/7/GRCh38#138905513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38156272-C-A

138905637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157136-G-A

138905706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157243-T-A

138905855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157550-G-T

138905904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157595-T-C

http://identifiers.org/hco/7/GRCh38#138905936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38157635-A-C

138906031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157725-G-A

138906113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157814-C-T

138906232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157928-G-T

138906288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157972-G-A

138906317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38157999-A-G

138906809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158133-A-G

138906809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158133-A-T

138906823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158147-A-T

http://identifiers.org/hco/7/GRCh38#138906866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38158189-A-C

138906911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38158241-G-A

138906929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38158259-C-G

138906929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38158259-C-T

138906938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38158268-T-G

138907142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158472-A-G

138907163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158579-T-A

138907196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158643-T-G

138907315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38158786-G-A

138907503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159009-C-G

138907558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159056-G-C

138907560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159058-G-A

138907564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159062-T-A

138907564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159062-T-C

138907566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159064-T-A

138907657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159193-A-G

138907696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159229-G-A

138907835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159352-G-A

138907894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159423-C-T

138908231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159751-G-A

138908359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159882-T-G

138908410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38159923-C-T

138908525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160121-G-A

138908668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160416-A-G

138908730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160477-T-C

138908783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160536-T-C

138908837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160604-C-T

138908856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160627-T-C

http://identifiers.org/hco/7/GRCh38#138908863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38160634-A-C

138908863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160634-A-T

http://identifiers.org/hco/7/GRCh38#138908865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38160636-C-A

138908881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38160711-T-G

138909096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38161002-C-T

138909157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161066-G-T

138909166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161078-C-G

138909195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161095-G-A

http://identifiers.org/hco/7/GRCh38#138909222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38161117-C-A

138909223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161118-A-G

138909247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161142-G-C

138909247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38161142-G-T

138911130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167470-T-A

138911130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167470-T-C

138911130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167470-T-G

http://identifiers.org/hco/7/GRCh38#138911137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38167477-C-A

138911137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167477-C-T

http://identifiers.org/hco/7/GRCh38#138911177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38167517-A-C

138911177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38167517-A-G

138911177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38167517-A-T

138911180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38167520-G-A

138911180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38167520-G-T

138911335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167675-A-G

138911370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167714-G-T

138911414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167742-A-T

138911464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167792-G-A

138911473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167801-T-C

138911512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38167835-A-T

138911672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38168010-C-T

http://identifiers.org/hco/7/GRCh38#138911682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38168019-C-A

138911823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38168147-A-G

138911978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38168271-A-G

138912022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38168326-G-A

138912384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38168623-T-G

138913227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38169084-T-A

138913232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38169089-C-G

138913786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38169980-T-C

http://identifiers.org/hco/7/GRCh38#138916576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38171151-A-C

138916600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171171-G-A

138916600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171171-G-T

138916603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171174-G-A

138916603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171174-G-C

138916608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171179-G-C

138916608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171179-G-T

138916611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171182-T-C

138916618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38171195-A-G

http://identifiers.org/hco/7/GRCh38#138916672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38171245-A-C

138916998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38171587-T-C

138917012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38171601-G-A

138917113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: stop gained
orthologous variants: 38171699-A-T

138917134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38171720-G-A

138917142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38171728-G-A

138917153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38171739-G-A

138917169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38171755-G-A

http://identifiers.org/hco/7/GRCh38#138917225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/6/GRCm39#38171811-C-A

http://identifiers.org/hco/7/GRCh38#138917231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38171817-A-C

138917259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38171848-T-C

http://identifiers.org/hco/7/GRCh38#138917606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38172198-C-A

138917811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38172403-G-A

138917811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172403-G-C

http://identifiers.org/hco/7/GRCh38#138917856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38172448-C-A

138917856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38172448-C-T

138917861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172453-A-G

http://identifiers.org/hco/7/GRCh38#138917863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38172455-A-C

138917863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172455-A-G

138917921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172513-A-G

138917964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38172556-G-T

138917992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172584-T-G

http://identifiers.org/hco/7/GRCh38#138918046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38172635-C-A

138918046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172635-C-G

138918046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172635-C-T

138918073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172662-G-C

138918149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172738-G-C

138918155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38172744-C-T

138918450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173036-T-C

138918492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173078-T-C

138918503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173089-T-C

138918553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173142-T-C

138918670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173259-G-T

138918714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173303-C-G

138918714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173303-C-T

http://identifiers.org/hco/7/GRCh38#138918739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38173331-C-A

138918739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173331-C-T

138918798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173387-A-G

138918939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173528-G-A

138919086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173672-G-A

138919086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173672-G-C

138919100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173686-G-T

138919170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173756-G-A

138919200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous variant
orthologous variants: 38173786-G-A

138919288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173874-G-A

138919337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38173923-T-C

138919442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38174028-T-C

138919509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38174094-A-T

138919513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38174098-G-A

138924028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38174991-A-G

138924050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175013-T-G

http://identifiers.org/hco/7/GRCh38#138924215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38175125-C-A

138924215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175125-C-G

138924215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175125-C-T

138924235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175145-A-G

138924235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175145-A-T

138924248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175173-G-A

138924248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175173-G-T

138924267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175192-C-T

138924323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175247-T-C

138924517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175638-G-C

138924517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175638-G-T

138924548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38175657-G-C

138924895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176017-G-C

138924936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176058-G-A

138924947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176071-G-C

138924947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176071-G-T

138924956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176083-C-T

138925047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176167-C-T

138925135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176233-G-A

138925213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176299-G-A

138925926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176701-G-C

138925927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176702-G-C

138925957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176727-C-G

138925957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176727-C-T

138926080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176832-T-C

138926135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38176900-T-C

138926136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38176901-G-C

138926161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176926-C-T

138926220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38176977-A-G

138926686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38177108-T-G

138926687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38177109-G-C

http://identifiers.org/hco/7/GRCh38#138926734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38177152-C-A

138926815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38177230-A-T

138932221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38178582-G-C

138932390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38178718-A-G

138932621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179150-T-C

138932698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179198-G-A

138932796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179292-C-T

138932838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179334-A-T

138932954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179440-G-C

138933024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179497-C-G

138933368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38179736-C-T

138934574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38182605-A-G

http://identifiers.org/hco/7/GRCh38#138934729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38182785-C-A

138934968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38183356-A-G

138934988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38183374-C-T

138935204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38183585-A-G

138935272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38183648-C-T

138935636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron_variant, undefined
orthologous variants: 38183999-T-C

138936403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38184824-C-G

138936526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38184945-T-C

138937313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38188907-C-T

138937416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38189005-G-T

http://identifiers.org/hco/7/GRCh38#138938030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38190944-C-A

138938030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38190944-C-T

138938115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191022-G-A

138938115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191022-G-C

138938441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191338-C-T

138938535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191422-C-T

138938840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191769-G-C

138938940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38191858-T-C

138939241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192359-T-C

138939557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192647-T-C

138939563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192653-G-A

138939590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192680-A-G

138939610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192700-G-A

138939628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192718-T-A

138939668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192753-T-C

138939815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38192912-T-C

http://identifiers.org/hco/7/GRCh38#138939846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38192942-C-A

138941154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193013-C-T

138941155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193014-A-G

138941251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193108-T-C

138941359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193210-C-T

http://identifiers.org/hco/7/GRCh38#138941414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38193264-C-A

138941414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193264-C-T

138941534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38193368-A-G

138941765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38194486-T-C

138942613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196223-G-A

138942927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196233-G-A

http://identifiers.org/hco/7/GRCh38#138942932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38196238-A-C

http://identifiers.org/hco/7/GRCh38#138943046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38196345-C-A

138943180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196459-G-C

138943535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196878-G-A

138943569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196901-G-A

138943569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38196901-G-C

138943759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197019-G-A

138943777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197038-A-G

138943950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197174-A-G

138943950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197174-A-T

http://identifiers.org/hco/7/GRCh38#138944300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38197445-C-A

138944300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197445-C-T

http://identifiers.org/hco/7/GRCh38#138944348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38197490-C-A

138944360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197501-C-G

138944374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197515-T-C

138944426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197569-G-A

138944520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38197643-C-T

138944676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198192-G-A

138944677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198193-G-A

138944699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198215-T-A

138944785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198334-C-T

138944851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198400-G-C

138944881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198432-G-C

138944883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38198434-G-A

138945980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201122-T-C

138946151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201297-A-T

http://identifiers.org/hco/7/GRCh38#138946182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38201323-C-A

138946182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201323-C-T

138946273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201414-G-A

138946341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201482-C-G

138946808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201718-C-T

138946927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38201818-C-T

138947115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38202021-T-C

http://identifiers.org/hco/7/GRCh38#138947171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38202070-A-C

138947171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38202070-A-G

138947237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38202138-A-G

138947476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38202380-G-A

138948278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38203219-C-G

138950052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38207704-G-A

138950052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38207704-G-C

138950930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209276-A-G

138950950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209293-G-A

http://identifiers.org/hco/7/GRCh38#138951025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38209370-C-A

138951339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209468-T-C

138951365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209489-C-T

138951475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209619-G-A

138951630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38209740-T-A

138952857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211721-T-C

138952975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211820-C-T

138952976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211821-G-A

138952976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211821-G-C

138952976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211821-G-T

138953018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38211861-T-C

138953806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38212277-G-A

138956855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38216979-C-T

138956865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38216989-T-C

138957037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38217153-T-C

http://identifiers.org/hco/7/GRCh38#138957060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38217191-C-A

138957060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38217191-C-T

138957206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38217329-G-A

138958335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38217732-G-A

138963726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218537-A-G

138963851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218655-C-T

138963987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218787-C-T

138964076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218858-T-C

138964113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218895-C-T

138964183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38218966-C-T

138964389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38219125-G-A

138966836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38220819-C-T

138967027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38220992-T-C

138967087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38221042-A-G

138967381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38221286-G-C

http://identifiers.org/hco/7/GRCh38#138967667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38221718-C-A

138967667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38221718-C-T

138967742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38221834-T-G

138970229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38222130-T-G

138970595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38222454-G-A

138970793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38222723-T-A

138975072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38224219-G-C

138975420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38225134-C-G

138975420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38225134-C-T

http://identifiers.org/hco/7/GRCh38#138975591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38225249-A-C

138975692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38225327-A-G

138975725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38225362-G-A

138977364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38227016-G-A

138977610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38227441-T-C

138977634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38227465-C-T

138977652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38227483-G-A

138977652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38227483-G-C

138978438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228097-A-G

138978482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228141-T-A

138978532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228267-A-G

138978838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228527-C-T

138978879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228584-C-T

138978978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228676-G-A

138978978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228676-G-T

138979087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228777-G-A

138979170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228866-T-A

138979284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38228966-G-A

138979368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229050-G-C

138979655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229302-T-C

138979664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229312-C-T

138979806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229480-G-A

138979885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229578-T-C

138979960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229651-G-A

138979960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229651-G-C

138979975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229666-C-T

138980029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229724-G-A

138980043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229738-G-A

138980158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38229856-C-T

138980408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38230110-G-T

138980645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: intron variant
orthologous variants: 38230346-G-A

138981152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38230872-G-A

138981152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38230872-G-C

138981152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38230872-G-T

138981203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: synonymous_variant, undefined
orthologous variants: 38230914-G-A

http://identifiers.org/hco/7/GRCh38#138981262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#38230961-C-A

138981262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38230961-C-G

138981262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22219
most severe consequence: missense variant
orthologous variants: 38230961-C-T