http://identifiers.org/hco/2/GRCh38#230712924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85721229-C-A

230712924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85721229-C-G

230712937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85721247-G-T

http://identifiers.org/hco/2/GRCh38#230713059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85721369-C-A

230713183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85721496-G-C

230713183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85721496-G-T

230713198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85721511-G-A

230713198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85721511-G-T

http://identifiers.org/hco/2/GRCh38#230713364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85721633-C-A

230713364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85721633-C-G

230713560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721727-G-T

230713575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721742-G-A

230713575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721742-G-T

http://identifiers.org/hco/2/GRCh38#230713619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85721790-C-A

230713619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721790-C-T

http://identifiers.org/hco/2/GRCh38#230713644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85721816-C-A

230713644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721816-C-T

230713645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721817-G-A

230713645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85721817-G-T

http://identifiers.org/hco/2/GRCh38#230713880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85722044-C-A

230713880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 85722044-C-T

230714166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85722344-T-C

230714354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85722534-A-G

http://identifiers.org/hco/2/GRCh38#230714546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85722725-C-A

230714546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85722725-C-T

230715346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85723770-T-C

230715427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85723851-A-G

230715967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85724546-G-A

230715991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85724567-T-C

230716334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85724854-T-C

230717775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85725338-C-G

http://identifiers.org/hco/2/GRCh38#230717832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85725387-A-C

230717944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85725502-C-T

230717946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85725504-T-C

230718064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85725754-A-G

230718131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85725876-T-C

230718603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85726340-A-G

230718892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85726603-G-T

230719528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85727436-T-C

230719880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85727734-G-T

230720056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85727900-T-G

230720934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85728388-C-T

230721077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85728663-C-T

230722723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85730382-T-C

230723170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85731018-G-C

230729919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85733548-A-G

230729989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85733656-G-A

230733104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85734582-A-T

230733151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85734621-A-G

230733262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85734711-A-G

230733265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85734714-T-C

230736926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85736173-T-C

230737773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85737141-C-T

230737807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85737176-A-G

230737919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85737271-G-T

230738122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85737479-T-G

http://identifiers.org/hco/2/GRCh38#230738124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85737481-C-A

230738140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85737499-T-A

230739167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85738739-A-G

230739356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85739382-G-A

230739380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85739402-G-T

230739431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85739442-A-G

http://identifiers.org/hco/2/GRCh38#230740298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85740608-C-A

230740574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85740834-C-G

230740574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85740834-C-T

230741022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85741135-G-T

230751461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85743545-G-T

http://identifiers.org/hco/2/GRCh38#230751735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85743705-C-A

230751753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85743723-G-C

http://identifiers.org/hco/2/GRCh38#230751923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85743848-A-C

http://identifiers.org/hco/2/GRCh38#230752027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85743946-C-A

http://identifiers.org/hco/2/GRCh38#230752031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85743950-C-A

230752031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85743950-C-T

http://identifiers.org/hco/2/GRCh38#230752312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85744076-A-C

230752312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85744076-A-G

230752397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85744134-T-G

230752489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85744181-A-G

230752599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85744282-C-G

230757425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745101-G-A

230757512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745171-A-G

230759416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745448-G-T

230759450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745482-G-T

230759453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745485-G-A

230759826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745795-T-C

230759844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745813-A-G

230759844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745813-A-T

230759848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85745817-T-C

230759936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85746055-A-G

230759940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85746059-A-G

230760157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85746273-G-A

230760157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85746273-G-T

http://identifiers.org/hco/2/GRCh38#230760164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85746280-C-A

230760164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85746280-C-T

230761648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85747719-A-G

230761702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85747771-G-A

230761804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85747859-G-A

230765294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85749744-A-G

230765529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85749963-C-T

230765798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85750206-C-T

230767951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85750729-A-G

230773465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85752371-G-A

230773509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85752411-T-C

230774721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85753419-C-T

http://identifiers.org/hco/2/GRCh38#230774848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85753532-C-A

230778994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 85754468-G-T

230779028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85754504-G-T

230779052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85754528-T-C

230779086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85754561-A-G

230779120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85754593-G-T

http://identifiers.org/hco/2/GRCh38#230779229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85754708-C-A

230779791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85755191-A-T

230779874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85755227-A-G

http://identifiers.org/hco/2/GRCh38#230782525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85756375-C-A

230783509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85757253-C-G

230783607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85757411-T-A

230783607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85757411-T-C

http://identifiers.org/hco/2/GRCh38#230783674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85757563-A-C

230783944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85757862-T-G

230784478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85758353-G-C

230786390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85758995-T-C

230786511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85759109-T-C

230786543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85759138-C-T

http://identifiers.org/hco/2/GRCh38#230787268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85760086-A-C

230787289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760133-C-G

230787352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760183-C-T

230787358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760189-A-G

230787584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760377-C-G

230787660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760436-C-G

230787887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760609-G-A

230787900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760622-G-C

230788260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85760986-T-A

230788516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85761226-C-T

230788795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85761540-A-G

230790781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85762955-A-T

230790802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85762979-T-C

230790833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763010-G-A

230790833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763010-G-C

230790833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763010-G-T

230790940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85763112-G-T

230791048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763220-A-G

230791048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763220-A-T

230791145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763304-G-T

230791396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763440-T-G

230791527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763522-A-G

230791647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763633-A-T

230791768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763731-G-A

230791879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763816-A-G

230791953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763892-T-C

230791953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85763892-T-G

230793125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85764922-A-G

http://identifiers.org/hco/2/GRCh38#230793144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85764939-A-C

230793144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85764939-A-G

230793382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85765177-A-G

230793623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85765420-C-T

230793702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85765502-G-A

230793781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85765580-T-C

230794294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85766022-A-G

230794357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85766057-A-G

http://identifiers.org/hco/2/GRCh38#230794358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85766058-A-C

230794358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85766058-A-G

230796297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85767433-T-C

230796593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85767717-A-G

230797037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768087-T-C

230797471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768432-A-G

230797513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768476-T-G

http://identifiers.org/hco/2/GRCh38#230797542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85768506-A-C

230797542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768506-A-G

230797764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768710-G-A

230797775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768721-G-T

230797785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85768731-G-T

230797961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85769050-A-G

230798568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85769760-G-A

230798568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85769760-G-T

http://identifiers.org/hco/2/GRCh38#230798973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85770153-C-A

230799026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85770199-A-G

230799073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 85770249-G-A

230799193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85770375-G-T

230799252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85770437-T-A

http://identifiers.org/hco/2/GRCh38#230808385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85771170-C-A

230808454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85771238-G-A

230808454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85771238-G-C

230808627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85771472-T-G

230808688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85771537-A-T

230808955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85771805-A-G

230810161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772208-T-A

230810193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772238-G-A

230810333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772384-G-A

230810333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772384-G-T

230810445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772491-G-C

230810445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772491-G-T

230810449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772495-T-A

230810449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772495-T-C

230810561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85772610-G-T

230811468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85773436-G-A

230811468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85773436-G-C

230811468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85773436-G-T

230811478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85773447-T-G

230811964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85774119-T-C

230813380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85774430-C-G

230813800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85774939-A-G

230813906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 85775035-G-A

230814045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85775127-T-C

230814045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 85775127-T-G

230817777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 85776021-T-A

230817777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85776021-T-C

230817819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 85776063-T-G

http://identifiers.org/hco/2/GRCh38#230817910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85776157-A-C

230817910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776157-A-G

230817995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776224-A-G

230818005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776232-A-G

230818061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776266-A-G

230818061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776266-A-T

http://identifiers.org/hco/2/GRCh38#230818094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#85776309-C-A

230818094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776309-C-T

230818103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 85776318-T-C

230818308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776595-T-G

230818417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776695-A-G

230818495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776734-T-C

230818495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776734-T-G

230818500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776739-G-A

230818500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron variant
orthologous variants: 85776739-G-T

230818512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 85776750-G-A

230818512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 85776750-G-T

230818533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: synonymous variant
orthologous variants: 85776771-T-A

230818620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: synonymous variant
orthologous variants: 85776858-G-A

230818620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: synonymous variant
orthologous variants: 85776858-G-C

230818620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: synonymous variant
orthologous variants: 85776858-G-T

230818709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85776947-C-T

230818795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85777031-A-G

230819143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85777347-G-C

230819143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85777347-G-T

230819429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85777618-A-G

230819731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85777920-T-C

230819938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778139-A-G

230820373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778574-T-C

230820460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778683-A-G

230820551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778769-G-A

230820551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778769-G-T

230820586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778804-A-T

230820620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778838-C-T

230820758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85778975-G-T

230820914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85779131-G-A

230820914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20292
most severe consequence: 3 prime UTR variant
orthologous variants: 85779131-G-C