http://identifiers.org/hco/3/GRCh38#58564151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14173463-A-C

58564197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173417-T-C

http://identifiers.org/hco/3/GRCh38#58564282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14173342-C-A

http://identifiers.org/hco/3/GRCh38#58564374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14173268-C-A

58564413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173229-G-T

58564414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173228-C-G

58564448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173210-T-C

58564471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173188-G-A

58564679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173027-G-A

58564702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14173004-A-G

58564752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172894-A-G

58565077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172446-A-G

58565135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172395-G-T

http://identifiers.org/hco/3/GRCh38#58565145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14172385-C-A

58565145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172385-C-T

58565146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172384-A-G

58565219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172306-G-T

58565229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172296-C-T

58565243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172282-T-C

58565243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172282-T-G

58565391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172139-G-T

58565466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172078-G-A

58565466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14172078-G-T

58565850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171788-T-C

58565859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171779-T-A

58565859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171779-T-G

58565900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171740-G-A

58565900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171740-G-T

http://identifiers.org/hco/3/GRCh38#58566014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14171633-C-A

58566033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171616-A-G

http://identifiers.org/hco/3/GRCh38#58566043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14171606-C-A

58566044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171605-A-G

58566044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171605-A-T

58566049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171600-G-A

58566049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171600-G-T

http://identifiers.org/hco/3/GRCh38#58566086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14171577-C-A

58566086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171577-C-G

58566086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14171577-C-T

http://identifiers.org/hco/3/GRCh38#58566418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14171214-C-A

58566418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14171214-C-T

58566663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 14171006-G-A

58566663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14171006-G-C

58566702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 14170967-G-A

58566729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170928-G-T

http://identifiers.org/hco/3/GRCh38#58566940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14170447-C-A

58566999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170395-G-T

58567009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170385-T-C

58567033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170356-C-G

58567033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170356-C-T

http://identifiers.org/hco/3/GRCh38#58567085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14170328-C-A

58567085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14170328-C-T

58567173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14170285-G-A

58567173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14170285-G-T

58567201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 14170268-C-T

58567274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 14170195-C-T

58567322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 14170147-T-C

58567380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170093-G-A

58567380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170093-G-T

http://identifiers.org/hco/3/GRCh38#58567385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14170088-C-A

58567412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170074-T-C

http://identifiers.org/hco/3/GRCh38#58567449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14170056-A-C

58567449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170056-A-T

58567494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170012-G-A

58567494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14170012-G-T

58567513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169992-T-A

58567513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169992-T-C

http://identifiers.org/hco/3/GRCh38#58567881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14169690-C-A

58568587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169487-T-C

58568674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169398-A-T

http://identifiers.org/hco/3/GRCh38#58568751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14169340-C-A

58568751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169340-C-T

58568775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169316-G-A

58569172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169082-C-T

58569185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169070-A-G

58569239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14169017-G-A

58569460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168834-A-T

58569602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168771-G-A

58569602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168771-G-C

58569602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168771-G-T

58569608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168765-T-A

58569611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168762-G-A

58569611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168762-G-T

http://identifiers.org/hco/3/GRCh38#58569616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14168757-C-A

58569616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168757-C-T

58569678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168724-G-A

58569678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168724-G-T

http://identifiers.org/hco/3/GRCh38#58569807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14168596-C-A

58569807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 14168596-C-G

58569809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14168594-G-A

58569809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14168594-G-C

58569896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168507-G-A

58569914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168494-C-T

58569926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168482-G-T

http://identifiers.org/hco/3/GRCh38#58569929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14168479-C-A

58569929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168479-C-T

http://identifiers.org/hco/3/GRCh38#58569931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14168477-C-A

58569993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168428-G-T

58570138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14168278-A-G

58570212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167372-G-T

58570254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167330-A-G

58570265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167321-G-A

58570265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167321-G-C

58570280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167264-G-C

58570280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14167264-G-T

58570538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14167004-T-A

http://identifiers.org/hco/3/GRCh38#58570666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14166849-C-A

58570678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166837-C-T

58570736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166754-G-T

58570801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166618-G-A

58570801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166618-G-T

58570811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166608-G-A

58570811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166608-G-C

58570913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166503-A-G

58570957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14166459-C-T

58571526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165578-T-C

58571640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165279-T-C

58571660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165259-C-G

58571798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165135-G-A

58571846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165085-G-A

58571866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14165065-C-T

58571988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14164940-T-C

58572022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14164897-C-T

58572151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14164778-G-T

58572165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14164764-A-G

58572647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14164387-T-A

58572768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14164264-T-A

58572870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14164197-G-A

58572870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14164197-G-T

58572926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14164138-T-A

58572926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14164138-T-C

58573148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14163972-G-A

58573190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14163954-C-T

58573282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14163868-C-T

58573324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14163824-A-T

58573392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163759-G-A

http://identifiers.org/hco/3/GRCh38#58573421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14163635-C-A

58573421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163635-C-T

58573426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163629-T-C

58573433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163622-G-A

58573458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163597-G-T

58573528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163537-G-A

58573528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163537-G-T

http://identifiers.org/hco/3/GRCh38#58573551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14163518-A-C

58573551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163518-A-G

58573555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163514-G-A

58573555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163514-G-T

58573561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163508-A-G

58573581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163488-G-C

58573581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163488-G-T

58573590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163479-G-A

58573590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163479-G-T

58573655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163443-G-T

58573784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163360-G-A

58573784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163360-G-T

58573787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163357-C-T

58573871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163349-A-G

58574016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163301-G-A

58574112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163205-G-T

58574253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163078-G-A

58574263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14163068-C-T

58574319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162833-T-C

58574366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162790-A-G

58574462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162693-C-T

58574507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162649-G-T

58574607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162581-A-T

58574670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162509-G-A

http://identifiers.org/hco/3/GRCh38#58574705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14162478-C-A

58574705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14162478-C-T

58575052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14162111-C-G

58575129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14162034-C-T

58575137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14162026-G-A

58575221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161952-A-G

58575502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161690-T-A

58575719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161485-G-A

58575785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161441-C-T

58576137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161210-T-G

58576360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161020-A-G

58576370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14161010-G-A

58576522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160877-G-T

58576662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160755-C-G

58576723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160700-T-C

58576840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160627-C-T

58577106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160322-C-T

58577147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160289-C-T

58577177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160265-T-C

58577193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160248-A-T

58577232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160209-T-A

58577232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160209-T-C

http://identifiers.org/hco/3/GRCh38#58577267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14160175-C-A

58577267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160175-C-T

http://identifiers.org/hco/3/GRCh38#58577277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14160165-C-A

58577284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160158-T-C

58577299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14160143-A-G

58577475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159972-T-C

58577631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159815-A-G

58577653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159793-C-G

58577671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159759-G-A

58577671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159759-G-C

58577671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14159759-G-T

58577791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14159655-G-T

http://identifiers.org/hco/3/GRCh38#58578625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14159088-A-C

http://identifiers.org/hco/3/GRCh38#58578685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14159030-A-C

58579174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14158489-G-C

58579205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14158459-G-A

58579238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14158424-G-A

58579276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14158386-G-T

58579337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14158341-C-T

58580130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 14157044-A-G

58580858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14156490-G-C

58581305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155927-G-A

58581603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155692-C-T

58581774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155501-G-A

58581775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155500-C-T

58582105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155240-T-C

58582156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155204-C-G

58582156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14155204-C-T

58582412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154979-T-G

58582423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154967-G-A

58582428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154962-C-T

58582721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154706-T-C

58582766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154669-A-G

58582768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154667-T-G

58582788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154647-G-C

58582790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154645-G-A

58584124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14154162-G-A

58584300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14153988-C-T

58584307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14153978-C-T

58584401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14153867-C-T

http://identifiers.org/hco/3/GRCh38#58585383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14153330-C-A

http://identifiers.org/hco/3/GRCh38#58585387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14153326-C-A

58585567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, undefined
orthologous variants: 14153149-G-T

58585602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14153114-G-A

http://identifiers.org/hco/3/GRCh38#58585639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#14153078-C-A

58585651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, undefined
orthologous variants: 14153066-G-A

58585723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, undefined
orthologous variants: 14153025-C-T

58585791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152946-C-G

58586129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152656-T-C

http://identifiers.org/hco/3/GRCh38#58586222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14152575-C-A

58586233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152564-G-A

58586295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152500-A-G

58586731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152329-G-A

58586731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152329-G-T

58586732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152328-T-G

58586736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152324-G-A

58586736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152324-G-C

58586736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14152324-G-T

58586871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 14152253-C-T

58586945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152180-G-A

58586945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152180-G-T

http://identifiers.org/hco/3/GRCh38#58587014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14152136-C-A

58587014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152136-C-T

58587035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152115-G-A

58587035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152115-G-C

58587035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14152115-G-T

58587158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151988-G-C

58587158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151988-G-T

58587161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151985-A-G

58587161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151985-A-T

58587240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151946-T-C

58587286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151902-G-A

58587286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151902-G-T

58587619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151425-G-A

58587870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14151195-G-A

58592171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14149487-C-T

http://identifiers.org/hco/3/GRCh38#58596088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14148477-C-A

58596214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14148360-C-T

http://identifiers.org/hco/3/GRCh38#58596303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14148288-C-A

58596354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14148239-C-T

58597384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146971-G-A

58597411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146946-T-G

58597420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146937-A-G

http://identifiers.org/hco/3/GRCh38#58597465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14146891-A-C

58597685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146708-A-G

58597759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146636-C-T

58598041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146122-A-G

58598168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14146010-G-C

http://identifiers.org/hco/3/GRCh38#58598448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14145716-C-A

58598632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14145542-T-C

http://identifiers.org/hco/3/GRCh38#58598691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14145487-C-A

http://identifiers.org/hco/3/GRCh38#58598775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14145400-C-A

58598960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14145133-A-G

58598964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14145129-G-A

58599052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14144996-C-T

58599092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14144956-C-T

http://identifiers.org/hco/3/GRCh38#58599097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14144951-A-C

58599132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14144918-G-A

58599322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14144667-C-T

58601626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14142567-T-G

58601656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14142537-T-C

58601779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14142412-G-C

58602316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14141897-C-T

58602687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14141520-T-A

58602708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14141489-T-C

58602714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14141454-A-G

58603279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140863-G-A

58603280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140862-A-T

58603308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140834-A-T

58603414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140763-G-A

http://identifiers.org/hco/3/GRCh38#58603464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14140706-C-A

58603987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140194-A-G

http://identifiers.org/hco/3/GRCh38#58604007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14140174-C-A

58604007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140174-C-T

http://identifiers.org/hco/3/GRCh38#58604033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14140148-C-A

58604033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140148-C-G

http://identifiers.org/hco/3/GRCh38#58604106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14140085-C-A

58604106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14140085-C-T

58604420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139831-G-T

58604512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139744-G-T

58604540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139718-T-C

58604546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139712-G-A

58604546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139712-G-T

58604942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139392-T-C

58605014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139276-C-G

http://identifiers.org/hco/3/GRCh38#58605015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14139275-A-C

58605252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14139025-C-T

58605317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron variant
orthologous variants: 14138967-C-T

58608716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138203-T-C

58608738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138181-A-G

58608738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138181-A-T

58608744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138175-G-T

58608759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138160-G-T

58608781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138138-G-A

58608781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138138-G-T

58608796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138123-G-A

58608796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138123-G-T

58608813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138106-G-A

58608813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14138106-G-T

http://identifiers.org/hco/3/GRCh38#58609058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14137863-C-A

58609058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137863-C-T

58609067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137854-G-C

58609144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137794-T-C

58609178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137768-T-C

58609201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137756-T-C

58609229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14137728-G-A

58609325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14137629-A-G

58609576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14137217-A-G

http://identifiers.org/hco/3/GRCh38#58609668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14137140-C-A

58609939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136917-T-C

58610004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136873-A-T

58610199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136707-G-A

58610300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136649-C-T

58610322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136616-G-T

58610335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136604-C-T

58610341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136598-C-T

58610379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136559-C-T

58610380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136558-G-C

58610566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136369-G-A

58610593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14136344-G-C

58617242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14134044-T-G

58617396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133888-C-T

58617525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-A

58617525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-C

58617525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133764-G-T

58617757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133547-T-A

58617762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133541-G-C

58617799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133514-G-T

58617929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133434-G-A

58618002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133372-G-A

58618061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133320-G-A

58618063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133319-G-A

58618063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14133319-G-T

58620051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131520-G-T

58620195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131371-G-T

58620406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14131240-C-G

58620667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130908-C-G

58620667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130908-C-T

58620700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130876-G-C

58620776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130794-C-G

58620776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130794-C-T

58621024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130592-G-T

58621056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130559-G-A

58621174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130442-G-A

58621354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14130298-G-T

http://identifiers.org/hco/3/GRCh38#58621438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14130218-C-A

http://identifiers.org/hco/3/GRCh38#58621439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14130217-C-A

58624129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128427-T-A

http://identifiers.org/hco/3/GRCh38#58624179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14128392-C-A

58624247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128322-G-C

58624251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128318-G-C

58624273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128296-A-G

58624284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128276-A-G

58624290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128270-C-G

58624298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128262-G-A

58624456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128131-G-A

58624522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128070-A-G

58624563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14128029-C-T

58626379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127936-T-C

58626632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127683-C-T

58626789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127599-C-T

58626791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127597-G-A

58626791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127597-G-C

http://identifiers.org/hco/3/GRCh38#58626811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127577-C-A

58626854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127538-G-A

58626854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127538-G-T

http://identifiers.org/hco/3/GRCh38#58626865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127527-C-A

58626865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127527-C-T

58626891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127503-G-A

58626900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127494-G-A

58626900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127494-G-T

58626905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127489-C-G

58626905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127489-C-T

58626921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127474-G-T

http://identifiers.org/hco/3/GRCh38#58626930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127466-C-A

http://identifiers.org/hco/3/GRCh38#58626943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127453-C-A

58626943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127453-C-G

58626943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14127453-C-T

http://identifiers.org/hco/3/GRCh38#58626990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127409-C-A

58626990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127409-C-T

58627020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127379-G-A

58627024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127375-G-A

58627024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127375-G-T

http://identifiers.org/hco/3/GRCh38#58627058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127342-C-A

58627058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127342-C-G

58627058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127342-C-T

58627060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127340-T-A

58627117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127328-G-A

58627117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127328-G-T

http://identifiers.org/hco/3/GRCh38#58627131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127314-C-A

58627131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127314-C-T

58627222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127242-C-T

58627311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127152-G-A

58627311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127152-G-T

58627320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127139-G-T

58627356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127117-T-C

58627356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127117-T-G

58627357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127116-A-G

58627373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127100-G-A

58627373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14127100-G-T

http://identifiers.org/hco/3/GRCh38#58627436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#14127064-C-A

58627436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127064-C-T

58627450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127053-G-A

58627450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127053-G-T

58627463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127040-G-C

58627464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127039-G-A

58627464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127039-G-T

58627468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127035-G-A

58627488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127021-G-A

58627488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127021-G-C

58627503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127006-A-G

58627506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14127003-T-C

58627545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30827
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 14126963-G-T