http://identifiers.org/hco/8/GRCh38#80968024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9752755-C-A

http://identifiers.org/hco/8/GRCh38#80968043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9752774-C-A

80968406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9753113-G-C

http://identifiers.org/hco/8/GRCh38#80968409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9753116-C-A

80968424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9753131-C-T

80968564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9753262-G-A

http://identifiers.org/hco/8/GRCh38#80968696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9753388-C-A

80968813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9753501-T-C

80971006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9754568-T-C

80971058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9754616-G-T

80971096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9754647-T-C

80971107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9754658-A-G

http://identifiers.org/hco/8/GRCh38#80971301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9754845-A-C

80971314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9754858-T-A

80971492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9755000-G-T

80971587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9755080-A-G

http://identifiers.org/hco/8/GRCh38#80971677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9755366-A-C

80971801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9755480-G-A

80971801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9755480-G-T

80973138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9755517-T-C

80973926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9756047-T-C

80973946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9756066-G-T

80974036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9756161-T-C

80974296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9756966-G-A

80974449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757096-A-T

http://identifiers.org/hco/8/GRCh38#80974475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9757126-C-A

80974498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757152-T-C

80974498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757152-T-G

80974659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757274-G-A

80974694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757292-A-G

80974706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757304-G-T

80974886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757444-C-T

80974950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757492-G-C

80974999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757533-T-C

80975039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757572-T-C

80975050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757583-T-C

80975127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757642-T-C

80975311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9757790-G-T

http://identifiers.org/hco/8/GRCh38#80975577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9758035-C-A

80975577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758035-C-T

http://identifiers.org/hco/8/GRCh38#80975602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9758058-A-C

80975904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758301-G-A

80976034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758418-A-G

80976063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758445-T-C

80976101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758480-G-A

80976101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758480-G-T

80976104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758483-G-T

80976208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758577-G-A

80976213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758582-T-A

80976213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758582-T-C

80976213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758582-T-G

80976220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758589-T-G

80976295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758635-T-C

80976295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758635-T-G

80976303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758648-G-T

80976325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758677-G-C

80976325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758677-G-T

http://identifiers.org/hco/8/GRCh38#80976331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9758680-C-A

80976331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758680-C-T

80976438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758755-G-T

80976454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758770-G-A

80976454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758770-G-T

http://identifiers.org/hco/8/GRCh38#80976496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9758802-C-A

80976496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9758802-C-T

80976565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9758848-G-C

80976565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9758848-G-T

80976633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9758910-T-A

80976778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 9759061-A-T

80976805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9759088-C-G

80976886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9759169-T-G

80976959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759243-C-T

http://identifiers.org/hco/8/GRCh38#80977117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9759347-C-A

80977117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759347-C-T

80979374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759487-G-A

80979374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759487-G-T

80979397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759507-A-G

80979421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759530-G-A

80979421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759530-G-C

80979537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759652-T-C

80979547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759662-G-A

80979554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759669-G-A

80979554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759669-G-T

80979753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759850-T-C

80979848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759901-A-G

80979879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759926-C-G

80979879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9759926-C-T

80980319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760305-A-G

80980332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760316-T-A

80980343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9760327-T-C

80980373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9760361-T-C

80980373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9760361-T-G

http://identifiers.org/hco/8/GRCh38#80980401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9761145-C-A

80980401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761145-C-T

80980450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9761194-A-G

80980548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761302-T-C

80980548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761302-T-G

80980595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761336-A-G

80980596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761337-T-A

80980596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9761337-T-C

80982315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762282-G-A

80982393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762335-C-G

80982468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762415-C-T

80982640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762569-A-G

80982674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762606-T-A

80982674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762606-T-C

80982733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762662-T-C

80983084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762818-G-C

80983084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762818-G-T

80983089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762822-T-C

http://identifiers.org/hco/8/GRCh38#80983108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9762838-C-A

80983201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762925-C-T

80983274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9762993-C-G

http://identifiers.org/hco/8/GRCh38#80983500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9763195-C-A

80983711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763372-A-G

80983759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763419-C-T

80983821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763471-A-G

80983997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763625-T-C

80984022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763640-T-C

80984058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763670-C-T

80984074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763679-G-T

80984105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763710-G-A

80984163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763770-C-T

80984164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763771-G-A

80984217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763825-C-T

80984254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9763856-T-C

80984409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764014-G-C

80984416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764021-A-G

http://identifiers.org/hco/8/GRCh38#80984452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9764049-A-C

80984527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764116-T-G

http://identifiers.org/hco/8/GRCh38#80984640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9764223-C-A

80984640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764223-C-T

http://identifiers.org/hco/8/GRCh38#80984653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9764227-A-C

80984653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764227-A-G

80984934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9764443-C-T

80985169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9764663-C-G

80985193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9764687-C-T

80985229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9764723-T-C

80985442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764917-A-G

80985489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764944-G-T

80985496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764951-G-A

80985496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764951-G-C

80985496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764951-G-T

80985515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764970-T-C

80985515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9764970-T-G

80985639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765072-T-C

80985655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765089-G-T

80985692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765134-T-C

80985811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765387-C-G

80985818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765394-T-A

80985845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765420-C-T

http://identifiers.org/hco/8/GRCh38#80985849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9765424-A-C

80986106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765662-G-C

80986151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9765697-C-T

80986398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766121-G-A

80986412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766135-G-C

80986439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766148-C-T

80986481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766190-C-G

http://identifiers.org/hco/8/GRCh38#80986532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9766238-C-A

80986534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766240-G-C

80986789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766477-T-C

80986789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766477-T-G

80986803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766493-T-C

80986803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766493-T-G

80986808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766499-A-G

80986824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766515-G-C

80986886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766558-A-G

80986943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766620-A-G

80987074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766733-A-T

80987248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766927-G-T

80987282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766960-C-T

80987291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766964-T-G

80987314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766986-G-A

80987323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9766995-G-C

80987491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9767124-A-G

80988103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9767355-A-G

80988145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9767396-A-G

80989400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9768206-T-C

80989712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9768425-G-A

80989838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9768532-G-A

80990146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9768751-G-A

80990597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769099-C-T

http://identifiers.org/hco/8/GRCh38#80990617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9769102-C-A

80990617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769102-C-T

80990718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769187-C-T

80991366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769671-G-A

80991366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769671-G-T

80991383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769688-T-A

80991419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769724-A-G

80991445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769733-C-T

80991453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769741-C-T

http://identifiers.org/hco/8/GRCh38#80991506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9769791-A-C

80991527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9769812-T-C

80991596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769883-T-C

80991596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769883-T-G

80991623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769909-T-A

80991624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9769910-A-T

80991801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770032-C-T

80991816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770043-C-T

80991851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770078-G-T

80991956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770198-C-T

80992084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9770325-G-A

80992260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770469-T-C

80992384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770555-G-C

80992490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770638-A-G

80992713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770819-C-T

80992764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770871-C-T

80992794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770898-T-C

80992867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770960-A-G

80992869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9770962-A-G

80992989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771053-T-G

80992996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771063-A-G

80993046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771086-T-C

80993048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771088-T-C

80993062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771102-G-A

80993062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771102-G-T

80993065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771105-T-C

80993080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771120-G-A

80993080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771120-G-T

http://identifiers.org/hco/8/GRCh38#80993090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771130-C-A

http://identifiers.org/hco/8/GRCh38#80993112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771152-C-A

80993112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9771152-C-G

80993126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 9771166-G-A

80993126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9771166-G-C

80993128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 9771168-T-A

http://identifiers.org/hco/8/GRCh38#80993320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771362-C-A

80993320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771362-C-T

80993321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771368-A-G

http://identifiers.org/hco/8/GRCh38#80993325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771372-C-A

80993325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771372-C-G

80993325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771372-C-T

http://identifiers.org/hco/8/GRCh38#80993348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771394-A-C

http://identifiers.org/hco/8/GRCh38#80993369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771403-C-A

80993369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771403-C-T

80993417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771443-G-T

80993419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771445-T-C

http://identifiers.org/hco/8/GRCh38#80993436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771462-C-A

80993436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771462-C-G

80993436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771462-C-T

http://identifiers.org/hco/8/GRCh38#80993437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9771463-C-A

80993443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771470-T-C

80993990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9771906-C-T

80994338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772342-C-T

80994531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772496-G-A

http://identifiers.org/hco/8/GRCh38#80994585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9772520-C-A

80994673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9772566-C-G

80994995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9772898-G-A

80995014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 9772919-T-C

http://identifiers.org/hco/8/GRCh38#80995339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9773153-C-A

80995356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773170-C-T

80995479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773261-A-G

http://identifiers.org/hco/8/GRCh38#80995706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9773458-A-C

80995836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773593-C-T

80996060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773791-T-C

80996122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773836-C-T

80996127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9773841-G-T

http://identifiers.org/hco/8/GRCh38#80996501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9774099-C-A

80996676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9774255-C-T

80996687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9774266-A-T

80997687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775619-G-A

80997739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775665-G-C

80997848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9775779-T-C

http://identifiers.org/hco/8/GRCh38#80998605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9776327-A-C

80998605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776327-A-G

80998646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9776366-T-C

80998695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776414-C-T

80999039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9776744-G-C

81002170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9778704-G-A

http://identifiers.org/hco/8/GRCh38#81002172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9778706-A-C

81002295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9778818-A-T

81002326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9778849-T-C

81002432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9779204-C-T

81002494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9779251-G-A

81003423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9779999-C-T

81003443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780018-A-G

81003492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780047-A-G

81003791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780300-T-C

http://identifiers.org/hco/8/GRCh38#81003907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9780393-A-C

81003925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780411-C-T

81003926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780412-G-A

81003972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780457-C-T

81003980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780465-A-G

81004081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780684-T-A

81004427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9780994-G-A

81004778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9781284-T-G

81004879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9781385-C-T

81005194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9781710-G-A

81005272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9781758-G-A

81006505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 9783043-C-T

81006574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9783091-G-A

81006753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9783266-G-A

http://identifiers.org/hco/8/GRCh38#81006895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9783401-C-A

81006895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9783401-C-T

81007020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9783524-C-G

81007347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9783811-C-T

81007673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784174-T-A

81007673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784174-T-C

81007694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784198-A-T

81008089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784648-A-G

81008205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784753-T-C

81008244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784792-A-G

81008284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784833-C-T

81008363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9784903-C-G

81008751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785182-T-C

81008891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785337-T-C

81008947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785401-G-T

81008950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785404-C-T

81009150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785600-C-G

81009150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785600-C-T

81009290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9785736-G-T

81009326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9786207-T-C

81009331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9786212-T-G

81009510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9786376-T-A

81010371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787221-G-T

81010576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787420-T-C

81011028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787836-C-G

81011028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787836-C-T

81011029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787837-G-A

81011099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787888-A-G

81011109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787898-T-C

81011120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9787909-G-A

81011613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9788187-T-G

81011875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9788443-T-C

81011876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9788444-G-T

http://identifiers.org/hco/8/GRCh38#81011983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9788539-C-A

81012348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9788845-C-T

81012371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9788868-T-C

81012492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9789158-C-G

http://identifiers.org/hco/8/GRCh38#81014186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9792979-A-C

81014186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9792979-A-G

81014349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9793107-T-C

81014497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9793257-G-A

http://identifiers.org/hco/8/GRCh38#81015007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9793720-C-A

81015317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794364-A-G

81015318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794365-T-C

81016271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794456-G-T

81016283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794468-C-T

81016652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794776-G-A

81016652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794776-G-T

81016725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794846-T-A

81016755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9794876-C-T

81016896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795000-C-T

81016934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795029-C-T

81016991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795085-G-C

http://identifiers.org/hco/8/GRCh38#81017087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9795139-C-A

81017087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795139-C-T

81017222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795285-A-G

http://identifiers.org/hco/8/GRCh38#81017315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9795366-C-A

81017315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795366-C-T

81017455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795557-C-T

81017559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9795646-A-G

81018094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9796098-C-G

81018094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9796098-C-T

81018437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803546-C-T

81020703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803561-A-G

81020703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803561-A-T

81020704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803562-G-C

81021054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803910-C-G

81021054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803910-C-T

81021055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9803911-G-A

81021118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804019-G-A

81021152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804053-G-C

81021340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804226-G-A

81021343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804229-A-G

81021343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804229-A-T

81021351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804245-A-G

81021689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804646-G-A

81021812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804772-C-T

81021879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9804827-G-C

81022208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9805128-C-T

81022320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9805236-C-T

http://identifiers.org/hco/8/GRCh38#81022405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9805316-A-C

81022405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9805316-A-G

81022814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9805826-A-G

http://identifiers.org/hco/8/GRCh38#81025726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9814725-A-C

81025939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9814909-C-T

81025960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9814930-G-C

81026061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9815033-C-T

81026513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9815270-G-A

81028448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816025-G-A

81028529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816106-A-G

81028678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816245-T-C

81028690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816257-T-C

81028743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816304-C-G

81029018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816561-G-A

81029338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816899-T-C

http://identifiers.org/hco/8/GRCh38#81029396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9816936-C-A

81029415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9816955-T-G

81029509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9817047-C-T

http://identifiers.org/hco/8/GRCh38#81029790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9817282-C-A

81029790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9817282-C-T

81029798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9817290-A-G

81029834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9817325-T-C

http://identifiers.org/hco/8/GRCh38#81029861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9817352-C-A

81029861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9817352-C-T

http://identifiers.org/hco/8/GRCh38#81029937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9817410-C-A

81029943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9817416-C-T

81030070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9817527-G-T

81030124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9817590-G-C

81030183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9817647-C-T

81030563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9817983-C-T

81030752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818126-C-G

81030778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818156-C-T

81030897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818473-G-T

81031010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818592-T-C

81031060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818652-T-G

81031291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818864-G-A

81031339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9818910-T-G

81031499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819046-T-G

81031854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819435-T-C

81031946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819536-G-A

81032089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819657-T-C

81032236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819783-T-G

81032321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9819861-G-T

81033025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820493-T-C

81033080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820574-C-T

81033178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820708-T-C

81033250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820768-C-T

81033295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820794-T-C

81033484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820930-C-T

81033511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9820957-G-A

81033656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821076-A-T

81033697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821118-C-G

81033738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821151-C-T

81035424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9821241-G-C

81035475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9821300-C-T

81035707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821488-T-C

http://identifiers.org/hco/8/GRCh38#81035779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9821549-A-C

81035784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821554-T-A

81035844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821605-C-G

81036072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9821755-G-A

81036440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822093-T-C

81036440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822093-T-G

81036540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822200-T-C

81036602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822249-T-C

81036853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822450-G-A

81036853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822450-G-T

81037126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9822716-C-G

http://identifiers.org/hco/8/GRCh38#81037185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9822765-C-A

81037185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9822765-C-T

81037233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9822799-T-C

81037299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822865-T-A

81037351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822918-G-A

81037353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9822920-T-G

81037433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823007-G-A

81037589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823167-T-A

81037589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823167-T-C

81037736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823459-C-T

81037805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823517-T-A

81037923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823628-T-C

81038012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823701-G-A

81038012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9823701-G-C

81039379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9824462-G-A

81039379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9824462-G-T

http://identifiers.org/hco/8/GRCh38#81039388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9824471-C-A

81039405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9824502-G-T

81039468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9824547-A-G

http://identifiers.org/hco/8/GRCh38#81039641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9824721-C-A

81039669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9824748-T-C

81039686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9824763-G-A

81039686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9824763-G-C

81039686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9824763-G-T

81039819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9824886-C-T

81040026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825277-G-T

81040030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825281-A-G

81040084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825378-G-C

81040139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825442-G-A

81040202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825502-A-G

81040516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9825720-A-G

81040869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9826026-G-A

81040877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9826034-A-G

http://identifiers.org/hco/8/GRCh38#81041039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9826884-C-A

81041213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9827023-C-T

81041244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9827052-T-C

81041759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9827612-T-C

81042058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9827911-T-C

http://identifiers.org/hco/8/GRCh38#81042413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9829100-A-C

81042433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829111-T-C

81044359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829352-G-A

81044457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829447-T-C

81044521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829509-T-C

81044621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829605-G-A

81044659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829642-T-C

81044952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829912-A-G

81044953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9829913-G-A

81045263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9830164-G-T

http://identifiers.org/hco/8/GRCh38#81045276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9830177-C-A

81045307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9830191-T-A

81045620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9830441-G-A

81045620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9830441-G-T

81045973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9831504-C-T

81046052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9831577-G-C

81046176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9831707-G-A

http://identifiers.org/hco/8/GRCh38#81046451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9832087-C-A

81046451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832087-C-T

81046639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832300-G-A

81047523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832351-T-A

81047523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832351-T-C

81047587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832416-G-A

81047589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832418-G-C

http://identifiers.org/hco/8/GRCh38#81047613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9832446-A-C

81047633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832466-C-T

81047635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832468-C-T

http://identifiers.org/hco/8/GRCh38#81047637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9832470-C-A

81047637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832470-C-T

81047653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832485-T-C

http://identifiers.org/hco/8/GRCh38#81047803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9832628-C-A

81047803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9832628-C-T

http://identifiers.org/hco/8/GRCh38#81048188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9832960-A-C

81048218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9832990-C-T

81048260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833032-A-T

81048400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833145-G-C

81048452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833174-C-G

http://identifiers.org/hco/8/GRCh38#81048634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9833317-C-A

81048647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833330-T-A

81048647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833330-T-C

81048727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833409-C-T

81048758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833442-T-C

81048797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9833479-T-A

81048929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9833579-T-A

81049540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834082-T-C

81049616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834155-G-A

http://identifiers.org/hco/8/GRCh38#81049886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9834381-A-C

81049893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834388-T-C

http://identifiers.org/hco/8/GRCh38#81049986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9834479-C-A

http://identifiers.org/hco/8/GRCh38#81050260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9834736-A-C

81050260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834736-A-G

81050333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834804-C-T

81050437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9834901-G-A

81050615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9835156-G-A

81051264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9835434-C-G

81051349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9835512-C-T

81051564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9835727-T-C

81051592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9835753-G-A

81052480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9838543-G-A

81052609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9838672-G-C

81052621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9838684-G-C

81052765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9838802-C-T

81052981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839012-G-A

http://identifiers.org/hco/8/GRCh38#81053221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9839238-C-A

81053287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839294-T-G

81053421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839427-T-C

81053563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839530-T-A

81053563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839530-T-C

81053671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839655-T-C

81053747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839743-T-C

81053775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9839764-A-G

81054134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9840100-A-T

81059247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9841399-T-G

81059280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9841428-T-C

81059306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9841457-A-T

81059452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9841587-C-T

81059758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9841872-G-A

81060594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844339-T-C

81060729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844474-C-T

81060948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844660-T-C

81060950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844662-C-T

81061205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844891-T-A

81061314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9844988-G-A

81065042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9845337-T-A

81065042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9845337-T-C

81065350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9845560-A-G

81065390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 9845603-T-C

81065583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9845767-C-T

81065642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9845775-C-T

81065927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847039-C-T

81065936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847048-G-C

81065948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847058-G-A

81066049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847106-A-G

81066574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847558-C-T

81066714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847688-A-G

81066826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847796-G-C

81067248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9847953-T-C

http://identifiers.org/hco/8/GRCh38#81067455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9848128-C-A

81067487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9848156-T-A

81067644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9848313-G-C

81067644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9848313-G-T

81068062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9848553-A-G

81068847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9850244-T-C

81068939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9850337-C-G

81068939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9850337-C-T

81069066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9850460-C-T

81069540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9850979-A-G

81069641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9851054-C-T

81069672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9851082-C-T

81070036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9852244-G-T

81070078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9852286-G-T

81070427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852825-T-C

81070483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852912-A-T

81070566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852979-C-T

http://identifiers.org/hco/8/GRCh38#81070572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9852985-C-A

81070572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852985-C-G

81070572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852985-C-T

81070582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9852999-C-T

81070669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9853170-G-A

81070669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9853170-G-T

81070734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9853241-T-C

81070926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9853422-G-A

81071376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9853899-G-A

http://identifiers.org/hco/8/GRCh38#81073329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9858270-C-A

81073824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9858714-G-A

81073885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9858782-T-A

81074220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859239-C-T

http://identifiers.org/hco/8/GRCh38#81074249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9859268-A-C

81074254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859272-T-C

81074285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859302-T-C

81074360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859381-T-A

81074399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859418-G-T

81074428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859430-G-C

81074461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859461-T-C

81074461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859461-T-G

81074522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859501-G-A

81074677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9859630-T-G

http://identifiers.org/hco/8/GRCh38#81074796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9859756-C-A

81074810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859769-G-A

81074874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859809-C-T

81074931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9859866-G-A

81075013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9859923-T-G

81075120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860037-A-G

81075510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860463-C-T

81075615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860578-A-G

81075668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860624-G-A

81075712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860665-G-T

81075716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860669-C-T

81075726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860679-A-G

81075760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860706-C-T

81075952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9860889-G-A

81076076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9861021-A-G

81076192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9861117-T-C

81076431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9861327-C-G

http://identifiers.org/hco/8/GRCh38#81076507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9861402-A-C

81076897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9861739-T-C

81077213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9862050-A-G

81077282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9862119-T-C

81077348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9862178-C-G

81077554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9863276-G-A

81077572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9863300-A-G

81077680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9863400-T-C

81078293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9864548-T-A

81078395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9864649-T-A

http://identifiers.org/hco/8/GRCh38#81078403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9864661-C-A

81079096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9865150-T-C

81079443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9866005-G-A

http://identifiers.org/hco/8/GRCh38#81079479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9866040-C-A

81079479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9866040-C-T

81079582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9866136-C-G

81079582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9866136-C-T

81080745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9866670-T-A

81083461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9870523-G-A

http://identifiers.org/hco/8/GRCh38#81083597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9870632-A-C

81083624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9870654-G-A

81084147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9870859-G-T

81085049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871627-G-A

81085049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871627-G-C

81085049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871627-G-T

81085089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871669-G-T

81085118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871698-T-C

81085386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9871957-A-G

81085609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9872104-C-T

81085751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9872216-T-A

81085839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9872303-T-C

81085845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9872309-T-C

81085879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9872336-T-C

81087535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9873417-A-G

81087718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9873581-T-C

81087848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9873743-G-A

81088124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9874001-A-G

http://identifiers.org/hco/8/GRCh38#81088537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9874271-A-C

81089308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9874951-G-A

81089497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875111-G-T

81089594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875145-T-C

81089788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875322-G-A

81089825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875359-C-T

81090146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875649-T-C

81090257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9875947-T-C

81090310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9876003-G-A

81090310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9876003-G-C

81090558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876177-C-T

81090724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876335-T-G

http://identifiers.org/hco/8/GRCh38#81090751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9876362-C-A

81090751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876362-C-T

81090752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876363-T-A

81090786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876387-C-T

81090967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9876565-A-G

81091249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9876771-G-A

81091249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9876771-G-C

81091274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9876796-G-A

81092548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 9877228-A-G

81092782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9877433-A-T

81092890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9877550-G-A

81093209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9879597-G-A

81093320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9879718-C-T

81093428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9879819-T-C

81093583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9879963-G-A

81093583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9879963-G-C

http://identifiers.org/hco/8/GRCh38#81093721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9880101-A-C

81093829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880206-A-G

81094162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880442-C-T

81094169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880449-C-G

81094169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880449-C-T

81094304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880560-C-T

81094391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880646-C-T

81094500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880752-T-C

81094566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880816-T-C

81094634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880877-C-T

81094640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9880883-G-A

81097255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9882774-G-T

81097300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9882816-G-A

81098056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9883075-T-C

81098224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9883241-T-C

81098351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9883363-T-C

81098352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9883364-G-A

81098361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9883373-C-T

81098935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9886322-G-A

81099133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9886518-A-G

81099320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9886816-A-G

81099345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9886838-A-T

81099490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9886976-A-G

81099492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9886978-G-C

81099695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887243-T-C

81099747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887289-G-C

81099765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887322-T-C

81099843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887430-T-C

81099866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887447-T-C

81099873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887454-T-C

81099899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887479-C-G

81099916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887492-T-C

http://identifiers.org/hco/8/GRCh38#81099925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9887501-A-C

81099933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887510-T-C

81100007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887580-T-G

81100032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887602-T-G

81100823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887759-T-C

81100874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887795-T-C

http://identifiers.org/hco/8/GRCh38#81100930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9887847-C-A

81100930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887847-C-G

81100951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9887871-G-A

http://identifiers.org/hco/8/GRCh38#81101023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9887938-C-A

81101102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9888021-C-T

81101351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9888540-G-A

81101420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9888613-T-C

81101678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9888845-T-C

81101790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9888949-A-G

81102001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9889131-C-T

81102004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9889134-T-G

81102007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9889137-T-G

81102044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9889177-T-C

http://identifiers.org/hco/8/GRCh38#81102544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9889650-A-C

81102977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890084-G-A

http://identifiers.org/hco/8/GRCh38#81102994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9890101-C-A

81103171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890260-G-A

81103285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890368-T-A

81103315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890402-C-T

http://identifiers.org/hco/8/GRCh38#81103375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9890468-C-A

http://identifiers.org/hco/8/GRCh38#81103479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9890664-C-A

81103479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890664-C-G

81103479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9890664-C-T

81103847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891112-C-T

81103848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891113-G-A

81103892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891155-T-G

81103973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891230-T-C

81104204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891386-C-T

81104264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891444-C-T

81104295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891475-C-T

81104412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9891580-C-T

81104413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9891581-G-A

81104413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9891581-G-C

81104413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9891581-G-T

81104438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891607-A-G

81104572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891826-G-A

81104655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891909-G-C

81104704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9891962-T-A

81104810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892049-T-C

81104864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892101-A-T

81105501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892722-C-T

81105557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892757-G-C

81105625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892826-A-G

81105784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892961-T-C

81105854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9892996-G-A

81105959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9893084-C-T

81106572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9893319-G-A

http://identifiers.org/hco/8/GRCh38#81106751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#9893568-C-A

81106751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9893568-C-T

81107070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9893861-G-A

81107070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9893861-G-T

81107095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9893886-T-C

81107261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894067-T-A

81107286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894085-G-A

81107381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894119-T-C

81107450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894162-T-C

http://identifiers.org/hco/8/GRCh38#81107479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9894182-A-C

http://identifiers.org/hco/8/GRCh38#81107554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9894250-A-C

81107562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894258-C-T

81107652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894361-G-C

81107654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894363-G-A

81107678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894387-A-G

81107763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894477-C-T

81107823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894502-T-C

81107823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894502-T-G

81107969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894647-C-T

http://identifiers.org/hco/8/GRCh38#81108215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9894987-C-A

81108215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9894987-C-T

81108293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9895061-G-A

81109007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9895780-C-T

81109015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9895788-C-T

81109098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9895869-G-T

81109231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9896030-G-A

http://identifiers.org/hco/8/GRCh38#81109411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9896194-A-C

81109745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9896490-C-T

81109803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9896548-A-G

http://identifiers.org/hco/8/GRCh38#81109988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9896677-A-C

81109988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9896677-A-G

81110185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9896864-C-T

81110657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897339-G-A

81110681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897363-A-G

81110741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897425-T-C

81110908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897596-G-C

http://identifiers.org/hco/8/GRCh38#81111109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#9897790-A-C

81111109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897790-A-T

81111194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9897875-G-C

81111459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9898140-G-A

81111459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 9898140-G-T

81111624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9898296-A-T

81111631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898303-T-C

81111686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898353-G-A

81111744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898402-A-G

81111830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 9898470-G-A

81111935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898577-G-A

81112029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898648-G-A

81112029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30043
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 9898648-G-C