100573720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89279774-G-A

100573720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 89279774-G-T

100573755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89279742-C-T

100573770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89279732-G-T

http://identifiers.org/hco/12/GRCh38#100573773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89279726-C-A

100573773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 89279726-C-T

http://identifiers.org/hco/12/GRCh38#100573798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89279701-C-A

100573798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279701-C-G

100573849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279649-C-T

100573880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89279610-C-T

http://identifiers.org/hco/12/GRCh38#100573882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89279608-C-A

100573882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89279608-C-G

100573901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89279591-G-A

100573901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89279591-G-T

http://identifiers.org/hco/12/GRCh38#100573928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89279564-C-A

100573928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279564-C-T

100574035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279452-G-A

100574035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279452-G-T

http://identifiers.org/hco/12/GRCh38#100574050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#89279438-C-A

100574050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 89279438-C-T

100574881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 89278696-G-A

100576570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278444-C-T

100576603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278427-G-A

100576603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89278427-G-T

http://identifiers.org/hco/12/GRCh38#100576840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89278028-C-A

100577514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276474-T-C

100577522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276466-T-G

100577529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276459-A-G

100577529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89276459-A-T

http://identifiers.org/hco/12/GRCh38#100577548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89276436-A-C

100582813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275996-G-C

100582875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275933-A-G

100582916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275897-G-A

100582923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275890-A-G

100582969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275839-C-G

100583179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275728-C-T

100583283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275626-T-G

100583401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89275516-C-T

http://identifiers.org/hco/12/GRCh38#100591599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89272602-A-C

100591696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89272521-A-G

http://identifiers.org/hco/12/GRCh38#100591726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89272491-C-A

http://identifiers.org/hco/12/GRCh38#100591767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89272452-A-C

100591817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89272402-T-C

100591939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89272278-T-C

100591991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89272225-A-G

http://identifiers.org/hco/12/GRCh38#100592000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89272216-A-C

100592074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89272141-T-C

100592218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89272088-C-T

http://identifiers.org/hco/12/GRCh38#100592428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89271903-C-A

100592428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89271903-C-T

http://identifiers.org/hco/12/GRCh38#100592829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89271687-A-C

http://identifiers.org/hco/12/GRCh38#100592881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89271636-C-A

100593008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89271513-A-G

100593091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89271440-A-G

100593145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89271386-G-T

100593267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89271252-A-G

100593509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270928-A-T

100593526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270911-G-A

100593586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270851-G-A

100593643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270794-C-T

100593681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270735-G-T

100593752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270672-C-G

100593798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270626-T-G

http://identifiers.org/hco/12/GRCh38#100593813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89270611-C-A

100593824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270599-G-T

100593955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270489-T-A

100593955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89270489-T-C

100594020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89270427-G-A

100594099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89270381-A-G

100594213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89270289-C-T

100594315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89270187-G-C

100594423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89270067-T-G

100594525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269973-A-G

100594651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269901-T-C

100594654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269898-A-G

100594667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269887-T-C

100594671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269883-G-A

http://identifiers.org/hco/12/GRCh38#100594695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89269858-C-A

100594695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269858-C-T

100594703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269849-A-G

100594756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269796-G-T

100594805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89269738-A-G

100594823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89269721-G-A

100594823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89269721-G-T

100594888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5 prime UTR variant
orthologous variants: 89269659-T-C

100594888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5 prime UTR variant
orthologous variants: 89269659-T-G

http://identifiers.org/hco/12/GRCh38#100594945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89269602-A-C

100594945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269602-A-G

100594945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269602-A-T

100595016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269558-A-T

100595034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269538-A-G

100595117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269454-A-G

100595319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269316-T-C

100595408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269016-T-G

100595424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269000-G-A

100595424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89269000-G-T

100595603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268837-G-T

100595655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268787-A-G

100595770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268650-T-C

100595818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268605-G-T

100595845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268577-G-A

100595845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268577-G-T

100598942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89268131-C-G

100599149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267985-T-C

100599204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267954-A-G

100599243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267921-T-A

100599243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267921-T-C

100599259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267905-C-T

100599519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267668-A-G

100599523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267664-G-A

100599526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89267661-G-A

http://identifiers.org/hco/12/GRCh38#100599645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89267327-A-C

http://identifiers.org/hco/12/GRCh38#100599830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89267157-A-C

100600288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266986-G-C

100600288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266986-G-T

100600293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266981-A-G

100600315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266959-A-T

100600363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266931-T-A

100600363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266931-T-C

100600391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 89266903-G-T

100600469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 89266825-G-A

100600567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266727-T-C

100600590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266718-T-A

100600684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266644-G-A

100600684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266644-G-T

100600735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89266601-A-T

100601365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89265259-G-A

100601538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89265110-T-C

http://identifiers.org/hco/12/GRCh38#100601543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89265105-C-A

http://identifiers.org/hco/12/GRCh38#100601729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89264914-A-C

100601773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89264875-T-A

100601773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89264875-T-C

100602266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263800-T-C

100602435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263642-T-C

100610321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263402-T-C

100610365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263346-G-A

100610493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89263216-T-C

100610947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262799-C-G

100610964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262784-A-G

100611843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262563-T-C

http://identifiers.org/hco/12/GRCh38#100611891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89262514-C-A

100611958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262447-A-G

100611958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262447-A-T

100611981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262428-A-G

100611981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89262428-A-T

100611995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 89262414-T-C

100612011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 89262398-G-A

http://identifiers.org/hco/12/GRCh38#100612021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89262388-C-A

100612021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89262388-C-T

100612039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89262370-G-A

100612160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89262252-A-G

100612165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89262247-T-C

http://identifiers.org/hco/12/GRCh38#100612173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89262239-A-C

100612173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89262239-A-G

100612274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89262140-A-G

http://identifiers.org/hco/12/GRCh38#100612358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89262062-C-A

100612496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 89261946-G-T

100612575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261875-G-T

100612622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261274-G-T

100612664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261226-G-T

100612690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261201-G-A

100612793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261047-T-C

100612809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261033-G-A

100612833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89261019-C-T

100612962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260922-C-T

100613013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260867-C-T

100613199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260694-G-A

100613199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260694-G-C

100613316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260590-T-A

100613413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89260518-C-G

100616859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259311-A-G

100616868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259302-A-G

100616908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259262-G-A

100616909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259261-A-G

100616947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259209-G-A

100616957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259199-C-T

100616986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259172-C-T

100617033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259067-A-T

100617035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259064-G-A

100617035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259064-G-T

100617046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259051-A-T

100617076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89259036-A-T

100617121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258976-G-C

100617162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258930-C-T

100617232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258877-G-A

100617523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258354-C-G

100617523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258354-C-T

100617592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258288-G-A

100617723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258164-A-T

100617735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89258147-T-C

100618035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257846-G-A

100618035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257846-G-T

100618048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257833-T-C

100618049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257832-T-A

100618183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257723-G-A

100618353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89257555-T-G

100618450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 89257454-T-C

100618526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 89257378-G-A

http://identifiers.org/hco/12/GRCh38#100618576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89257328-C-A

100618576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 89257328-C-T

http://identifiers.org/hco/12/GRCh38#100618736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89257173-A-C

100618736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257173-A-G

100618736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257173-A-T

100618743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257166-G-A

100618743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257166-G-T

http://identifiers.org/hco/12/GRCh38#100618745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89257164-C-A

100618747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257162-T-C

100618749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257160-A-G

100618807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257104-G-A

100618807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89257104-G-T

http://identifiers.org/hco/12/GRCh38#100619022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89256904-A-C

100619390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89256569-G-T

100619428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89256520-G-T

100619487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89256460-G-T

100619501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89256446-G-T

100619533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255960-A-G

100619553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255940-A-G

100619872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255661-C-T

100619884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255649-G-C

100619956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255578-A-G

100619957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255577-G-A

100620016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255516-T-G

100620545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89255007-A-G

http://identifiers.org/hco/12/GRCh38#100620638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89254930-C-A

100620745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89254821-C-G

100620749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89254817-A-G

100621053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89254615-C-T

http://identifiers.org/hco/12/GRCh38#100621212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89254458-A-C

100621384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89254166-A-G

100621671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89253275-G-C

100622145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89253123-A-G

100622161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89253108-G-T

100622163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89253102-A-G

100622250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89253015-A-G

100622287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: missense variant
orthologous variants: 89252975-G-T

http://identifiers.org/hco/12/GRCh38#100622317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89252945-C-A

100622317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: stop gained
orthologous variants: 89252945-C-T

100622400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252862-A-G

http://identifiers.org/hco/12/GRCh38#100622463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89252798-C-A

100622463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252798-C-G

100622468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252793-T-A

100622488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252771-A-T

100622623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252630-G-C

100622643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252610-C-T

http://identifiers.org/hco/12/GRCh38#100622837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89252255-A-C

100622875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252204-C-T

100622967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89252101-C-T

100623370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89250562-T-A

100623417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89250521-A-G

100623417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89250521-A-T

100623486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: intron variant
orthologous variants: 89250429-A-G

100623849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89250065-T-C

http://identifiers.org/hco/12/GRCh38#100624099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89249839-C-A

100624099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249839-C-T

100624102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249836-A-G

http://identifiers.org/hco/12/GRCh38#100624120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89249818-C-A

100624120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249818-C-T

100624129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249809-C-G

100624179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89249759-C-T

100624201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249737-T-C

100624231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249707-C-T

100624424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249529-C-T

http://identifiers.org/hco/12/GRCh38#100624435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89249518-C-A

100624435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249518-C-G

100624435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249518-C-T

100624651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249302-G-A

100624651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89249302-G-T

http://identifiers.org/hco/12/GRCh38#100624710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89249243-C-A

100624710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89249243-C-G

100624710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89249243-C-T

100624815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89249138-A-G

100624902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89249051-T-A

100624902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89249051-T-C

100625012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248940-G-A

http://identifiers.org/hco/12/GRCh38#100625139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89248880-A-C

100625145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248874-T-C

http://identifiers.org/hco/12/GRCh38#100625202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89248815-A-C

100625202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248815-A-G

100625202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248815-A-T

100625223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248794-T-C

100625223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248794-T-G

100625402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248557-A-G

100625671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248237-G-A

100625743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89248174-G-A

100625902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89247604-C-T

100626129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89247386-G-A

100626280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246990-G-A

100626280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246990-G-T

100626290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246980-G-A

http://identifiers.org/hco/12/GRCh38#100626343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89246924-C-A

100626343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246924-C-T

http://identifiers.org/hco/12/GRCh38#100626407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#89246886-C-A

100626463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246834-A-G

100626466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246831-G-C

100626505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246792-T-A

100626553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246747-A-G

100626692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246598-T-C

100626818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246497-G-T

100626824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246491-T-C

100627689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89246035-G-T

100627781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245957-T-G

100627856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245872-T-C

100627952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245597-T-C

100628046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245383-G-A

100628180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245252-A-G

100628188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245244-A-G

100628219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245188-T-A

100628281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 89245131-C-G