http://identifiers.org/hco/11/GRCh38#66070634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5322773-C-A

66070634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5322773-C-G

66070634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5322773-C-T

66070727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5322680-G-A

66070727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5322680-G-T

http://identifiers.org/hco/11/GRCh38#66070772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5322635-C-A

66070772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5322635-C-T

66070832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5322575-T-C

http://identifiers.org/hco/11/GRCh38#66070910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5322483-C-A

66070910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322483-C-T

66070927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322466-T-C

66070927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322466-T-G

http://identifiers.org/hco/11/GRCh38#66070937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5322456-C-A

66070937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322456-C-T

http://identifiers.org/hco/11/GRCh38#66070949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5322445-C-A

66070949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322445-C-T

66071043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322348-C-T

66071219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322157-T-A

66071297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322083-G-A

66071334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5322058-G-T

66071589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321830-T-C

66071934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5321467-T-C

66072354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320926-C-G

66072368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320915-C-G

66072454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5320744-C-T

66073376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319738-A-G

http://identifiers.org/hco/11/GRCh38#66073423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5319705-A-C

66073484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5319490-G-A

66074821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5318228-C-T

66076195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317815-C-T

66076425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317718-G-A

66076708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317420-G-C

66076897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5317300-A-T

66078094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5313147-C-T

66080347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5309416-A-G

66081958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5307125-T-C

66082027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5306343-T-C

66083398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5305046-A-G

66083600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304839-C-T

66084026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5304410-A-G

66084026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5304410-A-T

66084187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5304106-A-G

http://identifiers.org/hco/11/GRCh38#66084222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5304073-C-A

http://identifiers.org/hco/11/GRCh38#66084236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5304059-C-A

66084236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304059-C-G

66084236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304059-C-T

http://identifiers.org/hco/11/GRCh38#66084243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5304047-C-A

66084243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5304047-C-T

66084587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5303641-G-A

66085044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5303252-C-T

http://identifiers.org/hco/11/GRCh38#66085240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5303106-A-C

66089236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5298471-T-C

http://identifiers.org/hco/11/GRCh38#66090047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5297276-C-A

66090147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5297189-A-G

http://identifiers.org/hco/11/GRCh38#66090857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5296724-C-A

66090858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5296723-A-G

66100220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5288905-C-G

66102020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5283068-T-C

66104172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281696-C-T

66104270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281631-T-A

66104512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5281288-A-G

66104925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280532-C-T

66104965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5280496-T-G

66105548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279172-A-G

66105659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5279111-T-C

66105841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278945-T-G

66105847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5278939-G-C

66107110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5276739-G-A

66109773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273647-C-T

66110217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5273197-G-C

66113582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263442-A-G

66113583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263441-G-A

66113806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5263246-A-G

66116090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5261417-C-T

http://identifiers.org/hco/11/GRCh38#66116092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5261415-C-A

66118003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260372-G-T

http://identifiers.org/hco/11/GRCh38#66118100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5260269-A-C

66118100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260269-A-G

66118140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260229-T-G

66118165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5260213-A-G

66124992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259164-T-C

66125046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5259118-G-A

66125709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258314-G-A

66125710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258313-G-A

66125750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258230-T-C

66125821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5258047-C-T

66125843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257954-C-T

66125946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257826-A-G

66125948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257824-G-A

66126019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257764-G-A

66126104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257682-T-C

66126111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257675-T-A

66126334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257522-G-A

66126334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5257522-G-T

66130113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254552-A-G

66130440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254221-G-A

66130452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5254214-T-C

66134147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249211-G-T

66134535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5249033-G-A

66134632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5248922-C-T

66134928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248650-C-T

66135693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248092-G-A

66135693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248092-G-C

66135693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5248092-G-T

66136022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247744-A-G

66136022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247744-A-T

66136198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247553-C-G

66136198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247553-C-T

66136232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5247531-G-A

66136822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246822-T-G

66136869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5246776-G-A

66139122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5245528-T-C

66140121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5245107-G-A

66140277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244957-G-C

66140277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244957-G-T

66140373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244917-T-C

66140375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5244915-A-G

http://identifiers.org/hco/11/GRCh38#66142870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5241768-A-C

http://identifiers.org/hco/11/GRCh38#66143272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5241365-C-A

66143288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241347-A-G

66143311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241329-A-G

66143311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241329-A-T

66143616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5241092-G-A

66144080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240961-T-A

66144333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5240716-G-A

66144726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5239381-C-T

66145151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238946-A-T

66145335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238798-T-C

66145544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5238643-G-A

66159899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5232050-A-T

66159983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231973-G-T

66160045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231929-A-G

66160085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5231889-T-A

66164234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226558-A-G

66164447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226358-A-T

66164457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226348-A-G

66164520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5226281-T-G

http://identifiers.org/hco/11/GRCh38#66164946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5225457-A-C

66164946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225457-A-G

66165061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225342-A-T

66165292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5225165-G-A

66166426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224748-C-T

66166465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224705-C-G

66166477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224693-G-A

66166478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224692-C-T

66166767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5224347-A-G

66167316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223882-T-C

66167632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5223566-T-C

http://identifiers.org/hco/11/GRCh38#66193450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5218071-C-A

66193450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5218071-C-T

66193550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5217973-G-C

66193656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217873-T-A

66193656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217873-T-C

http://identifiers.org/hco/11/GRCh38#66193661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5217868-C-A

66193661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217868-C-T

66193694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217846-G-A

66193694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217846-G-T

66193728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217813-C-T

66194486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217367-C-T

66194544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217309-A-G

66194694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5217163-A-G

http://identifiers.org/hco/11/GRCh38#66210458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5210737-C-A

66210458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5210737-C-T

66210560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210636-G-T

http://identifiers.org/hco/11/GRCh38#66210580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5210617-C-A

66210664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210521-C-T

66210985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210264-G-A

66210985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210264-G-T

http://identifiers.org/hco/11/GRCh38#66211051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5210208-A-C

66211051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210208-A-G

66211064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210195-G-A

66211064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210195-G-C

66211064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210195-G-T

66211096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210157-C-T

66211109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210142-C-G

66211109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5210142-C-T

http://identifiers.org/hco/11/GRCh38#66211325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5209958-C-A

66211325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209958-C-G

66211325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5209958-C-T

66213321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5208216-T-G

66213512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207915-G-A

http://identifiers.org/hco/11/GRCh38#66213521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5207906-C-A

66214189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207361-A-G

66214351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207211-G-A

66214351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5207211-G-T

66216026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206620-T-C

66216027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5206619-G-A

http://identifiers.org/hco/11/GRCh38#66216028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5206618-C-A

66216128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5206518-C-T

66216140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5206506-G-A

66216271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5206375-G-A

66216271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 5206375-G-C

66216344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5206134-T-C

66216386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5206092-T-G

66216503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5205990-T-G

66216606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5205887-G-A

http://identifiers.org/hco/11/GRCh38#66216620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5205873-C-A

66216620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5205873-C-G

66216620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5205873-C-T

66216664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5205825-C-G

66216853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205632-T-G

66216855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205630-G-C

66216855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205630-G-T

66216859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205626-A-G

66216859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205626-A-T

66216870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205615-A-T

66216975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205528-T-A

66216975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205528-T-C

66217017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205488-G-A

http://identifiers.org/hco/11/GRCh38#66217041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5205464-C-A

66217041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205464-C-T

66217134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205366-C-T

66217142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205361-G-T

http://identifiers.org/hco/11/GRCh38#66217358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5205189-C-A

66217425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205122-G-T

http://identifiers.org/hco/11/GRCh38#66217471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5205083-C-A

66217471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5205083-C-T

66217626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204899-G-A

http://identifiers.org/hco/11/GRCh38#66217694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204828-C-A

66217694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204828-C-G

http://identifiers.org/hco/11/GRCh38#66217723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204811-A-C

66217823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204725-T-C

http://identifiers.org/hco/11/GRCh38#66217834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204722-C-A

http://identifiers.org/hco/11/GRCh38#66217845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204711-C-A

66217845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204711-C-T

66217877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204679-T-C

http://identifiers.org/hco/11/GRCh38#66217892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204664-C-A

66217892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204664-C-T

66217990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204577-C-T

66218075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204513-T-A

http://identifiers.org/hco/11/GRCh38#66218393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5204235-C-A

66218427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5204191-A-T

66219358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5204073-C-T

66219466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203992-A-G

66219511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203952-A-T

http://identifiers.org/hco/11/GRCh38#66219539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5203928-C-A

66219596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 5203874-G-A

http://identifiers.org/hco/11/GRCh38#66219649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5203836-C-A

66219649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 5203836-C-T

66219886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203648-T-C

http://identifiers.org/hco/11/GRCh38#66219891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5203643-C-A

66219909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203625-G-A

66219909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203625-G-C

66219909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203625-G-T

http://identifiers.org/hco/11/GRCh38#66219948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5203589-C-A

66219951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203586-T-A

66220032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203478-G-A

66220035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203475-C-T

66220051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203463-G-A

66220073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203441-A-G

66220230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 5203333-C-T

http://identifiers.org/hco/11/GRCh38#66220363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5203186-C-A

66220363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5203186-C-T

66220442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5203067-G-A

66220442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5203067-G-T

66220520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5202971-G-A

66220520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5202971-G-T

http://identifiers.org/hco/11/GRCh38#66221004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5202527-C-A

66221004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5202527-C-G

66221004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5202527-C-T

http://identifiers.org/hco/11/GRCh38#66221043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5202501-C-A

66221043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5202501-C-G

66221080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5202467-A-G

http://identifiers.org/hco/11/GRCh38#66221305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5202241-C-A

66221305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5202241-C-T

66222163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5202141-G-A

66222189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5202112-A-G

66222313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5202024-G-A

66222349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201989-C-T

66222374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201964-A-G

66222427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201922-C-G

66222427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201922-C-T

66222567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5201823-C-T

66222813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201583-G-A

66222916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, undefined
orthologous variants: 5201466-G-A

66223684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5201156-T-C

66223725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5201116-T-C

66224698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5200476-G-A

66224756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5200420-C-T

66224907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5199537-G-A

66225626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5198953-T-C

66226281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5198668-G-A

http://identifiers.org/hco/11/GRCh38#66226460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5198502-C-A

66226805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5198212-A-G

66227189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5197710-A-G

66227192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5197707-G-A

66227266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5197552-A-G

66227497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 5197239-T-C

66227537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: missense variant
orthologous variants: 5197200-A-G

66227615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5197122-G-A

66227615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5197122-G-T

66227825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5196982-T-C

66228041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5196742-G-T

http://identifiers.org/hco/11/GRCh38#66228638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5196213-A-C

66228727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5196088-A-G

66228760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5196055-G-A

66228760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5196055-G-C

http://identifiers.org/hco/11/GRCh38#66230537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5195221-C-A

66230537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5195221-C-T

http://identifiers.org/hco/11/GRCh38#66230701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5195059-C-A

66230701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5195059-C-T

http://identifiers.org/hco/11/GRCh38#66230997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5194779-C-A

66230997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194779-C-T

66230999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194777-C-G

66230999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194777-C-T

66231053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194741-A-G

66231580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194411-A-G

66231598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194387-C-T

66231681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194304-T-C

66231681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194304-T-G

66231737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194250-G-A

66231737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194250-G-T

http://identifiers.org/hco/11/GRCh38#66231758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5194230-C-A

66231758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5194230-C-T

66231835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194156-T-A

66231835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194156-T-C

66231840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194151-G-A

66231840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194151-G-T

http://identifiers.org/hco/11/GRCh38#66231850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5194141-C-A

66231850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194141-C-G

66231850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194141-C-T

66231984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194031-T-C

http://identifiers.org/hco/11/GRCh38#66231998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5194018-C-A

66231998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 5194018-C-T

http://identifiers.org/hco/11/GRCh38#66232031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5193985-C-A

http://identifiers.org/hco/11/GRCh38#66232039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5193983-C-A

66232948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193488-T-G

http://identifiers.org/hco/11/GRCh38#66233132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5193316-A-C

66233132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193316-A-G

http://identifiers.org/hco/11/GRCh38#66233160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5193299-C-A

66233160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193299-C-G

66233160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193299-C-T

66233205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193252-T-C

66233410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5193060-C-T

66233672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5192803-G-T

66234018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192487-G-A

66234018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192487-G-T

66234035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192470-G-A

66234084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5192427-T-C

http://identifiers.org/hco/11/GRCh38#66235822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5191301-A-C

66235824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191293-A-G

http://identifiers.org/hco/11/GRCh38#66236026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5191102-C-A

66236026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5191102-C-G

66236358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190898-A-G

66236558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190697-G-A

66236558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190697-G-C

66236690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190594-A-G

http://identifiers.org/hco/11/GRCh38#66237567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5190382-C-A

66237581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190361-C-T

66237676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190267-C-T

66237777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5190101-G-T

http://identifiers.org/hco/11/GRCh38#66237990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5189959-A-C

66238081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189881-G-T

66238087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189875-G-A

66238096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189864-T-C

66238183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189806-G-T

66238370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189629-C-T

66238605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189511-A-T

66238704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189445-G-A

66238704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189445-G-T

http://identifiers.org/hco/11/GRCh38#66238727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5189422-C-A

66238727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189422-C-G

66238730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189419-A-G

66238730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189419-A-T

66238759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189388-T-C

66238784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189364-T-A

66238784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189364-T-C

66238784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5189364-T-G

66238876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189279-G-A

66238878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189277-G-A

66238878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189277-G-T

66238880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189275-G-A

66238880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189275-G-T

66238933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189239-T-C

66238933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189239-T-G

http://identifiers.org/hco/11/GRCh38#66238990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5189192-C-A

66238990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5189192-C-T

http://identifiers.org/hco/11/GRCh38#66239368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5188863-C-A

66239368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5188863-C-T

66239614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5188656-T-G

66240159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188094-A-G

66240159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5188094-A-T

66240421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187831-C-T

66240426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187826-G-A

66240602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187653-A-G

66240948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5187323-T-G

http://identifiers.org/hco/11/GRCh38#66241023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5187251-C-A

66241023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5187251-C-T

66241108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187204-A-G

66241114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187198-G-A

66241114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187198-G-C

66241114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187198-G-T

http://identifiers.org/hco/11/GRCh38#66241151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5187188-C-A

66241151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187188-C-T

66241180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187162-T-C

66241211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187140-T-C

66241222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187129-T-C

66241222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5187129-T-G

66241398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5186974-G-A

66241398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 5186974-G-T

66241692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5186691-A-G

66241884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5186395-T-C

66241903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5186376-A-G

66242435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5185698-C-G

66242435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5185698-C-T

66242574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5185564-A-G

66243053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: intron variant
orthologous variants: 5185131-G-T

66243393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184824-T-G

66243414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184805-C-G

66243414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184805-C-T

66243546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184696-G-A

66243546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184696-G-T

http://identifiers.org/hco/11/GRCh38#66243649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5184601-A-C

66243649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184601-A-G

66243916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184412-C-G

66243916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3 prime UTR variant
orthologous variants: 5184412-C-T

66243989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 5184347-T-C

66243989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 5184347-T-G

http://identifiers.org/hco/11/GRCh38#66244336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5184072-C-A

66244336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 5184072-C-T

66244453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30032
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 5183968-A-T