7541391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38335112-G-T

7541392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38335113-T-A

7541392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38335113-T-C

7541392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38335113-T-G

http://identifiers.org/hco/6/GRCh38#7541450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38335149-C-A

7541450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38335149-C-T

7541553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335240-G-A

7541553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335240-G-T

http://identifiers.org/hco/6/GRCh38#7541638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38335324-C-A

7541638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335324-C-G

7541638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335324-C-T

http://identifiers.org/hco/6/GRCh38#7541799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38335468-C-A

7541799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335468-C-T

7541987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38335636-G-A

7541987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38335636-G-T

http://identifiers.org/hco/6/GRCh38#7542098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38335783-C-A

7542098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335783-C-G

7542098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335783-C-T

7542182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38335869-G-A

7542215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38335911-T-C

7542215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38335911-T-G

http://identifiers.org/hco/6/GRCh38#7542232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38335933-A-C

7542232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38335933-A-G

7542338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336074-A-G

7542345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336081-G-A

7542387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336149-G-A

7542387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336149-G-T

7542409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336171-C-T

7542719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336434-G-A

7542719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336434-G-C

7542719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336434-G-T

7543003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38336707-C-G

7543032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336741-C-T

7543082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38336788-G-A

http://identifiers.org/hco/6/GRCh38#7543186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38336879-A-C

7543186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38336879-A-G

7543589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38337222-G-C

7543813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38337532-C-T

7543964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38337681-C-T

7544283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338007-G-A

7544388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338118-C-T

7544391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338121-T-G

7544478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338163-C-T

7544520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338190-A-T

7544529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338199-A-G

7544529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338199-A-T

7544695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338344-T-C

7545061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338744-A-T

7545124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338798-T-G

7545202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38338877-C-T

7545537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339147-T-G

7545964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339571-G-C

7546046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339647-C-G

7546227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339856-G-A

7546275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339906-T-C

7546336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339949-T-A

7546351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339964-G-A

7546351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38339964-G-T

7546553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38340245-G-A

7546805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38340490-T-C

7547174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38340862-C-T

http://identifiers.org/hco/6/GRCh38#7547230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38340928-A-C

7547250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38340956-T-G

7547577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38341273-C-T

7548304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38341748-A-T

http://identifiers.org/hco/6/GRCh38#7548322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38341766-A-C

7548418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38341868-C-G

7548517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38341935-G-T

7548776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38342306-G-A

7549113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38342570-A-G

7552694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344897-A-T

7552709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344910-G-A

7552777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344971-G-A

7552777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344971-G-C

http://identifiers.org/hco/6/GRCh38#7552804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38344999-A-C

7552804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344999-A-G

7552804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38344999-A-T

7553298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346116-G-A

7553391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346208-G-A

7553553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346627-A-G

7553603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346682-G-A

7553625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346703-A-G

7553750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346826-G-T

7553781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38346864-T-C

7553874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38346960-T-C

7554032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38347130-A-G

7554213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38347809-C-T

7555494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38348557-G-A

7555594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38348623-A-G

7555638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38348663-G-T

http://identifiers.org/hco/6/GRCh38#7555665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38348692-C-A

7555778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38348800-C-T

7555802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38348824-A-T

7555841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38348854-T-A

7555958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38348976-C-G

7555958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38348976-C-T

7556513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38349789-C-T

7556683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38349978-T-A

7556687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38349982-T-A

7556696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38349991-G-T

7556698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38349993-G-A

7556924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38350369-A-G

7558018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351400-T-C

7558037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351418-G-A

7558057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351437-C-G

7558079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351459-A-G

7558079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351459-A-T

7558084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351464-G-A

7558086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351466-G-A

7558086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351466-G-C

7558105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351481-T-C

7558220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38351596-A-G

7558293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351667-G-A

7558293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38351667-G-T

7558831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38352205-G-A

7559004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38352364-G-A

7559075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38352434-T-A

7559100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38352458-T-A

7559106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38352464-A-T

7559301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38352657-C-G

7559301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38352657-C-T

7559452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38352815-C-T

7559578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38352905-A-G

7559705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38352944-C-T

7560151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353293-C-G

7560254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353380-T-C

7560294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353420-A-T

7560349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353617-A-G

7560349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353617-A-T

7560426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38353827-A-G

7560657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38354085-A-T

7560713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38354151-C-G

7560788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38354230-G-A

7560812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38354258-G-A

7560869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38354308-G-A

7561288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38354611-G-A

http://identifiers.org/hco/6/GRCh38#7561445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38354754-C-A

7561590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38354906-G-A

7561590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38354906-G-T

7561711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38355014-T-C

7561900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38355200-G-C

7562082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38355392-T-G

7562158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38355469-A-G

7562541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356293-C-T

7562615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356718-A-T

7562627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356730-G-A

7562630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356734-T-A

7562630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356734-T-G

7562637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356741-G-C

http://identifiers.org/hco/6/GRCh38#7562684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38356787-C-A

7562684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38356787-C-T

7562813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356903-A-G

7562903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38356986-G-A

7562971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357051-T-G

7562999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357079-T-G

7563073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357162-C-T

7563498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357567-G-A

7563601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357661-A-G

7563718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38357776-C-T

http://identifiers.org/hco/6/GRCh38#7563836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38357871-C-A

http://identifiers.org/hco/6/GRCh38#7563886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38357964-C-A

7563929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358006-G-A

7563929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358006-G-T

7564283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358198-G-A

7564368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358277-T-A

7564403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358313-A-G

7564537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358462-C-T

7565172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358845-C-T

7565215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358883-G-A

7565215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358883-G-T

7565254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358924-G-A

7565254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38358924-G-T

7565334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38359020-T-A

7565337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38359023-T-C

http://identifiers.org/hco/6/GRCh38#7565348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38359033-C-A

7565348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38359033-C-T

http://identifiers.org/hco/6/GRCh38#7565448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/13/GRCm39#38359133-C-A

7565448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38359133-C-T

http://identifiers.org/hco/6/GRCh38#7565620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38359301-C-A

7565628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38359309-A-G

7566509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38360504-T-A

http://identifiers.org/hco/6/GRCh38#7566580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38360581-C-A

http://identifiers.org/hco/6/GRCh38#7566615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38360616-C-A

7566615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38360616-C-T

7566738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38360737-C-T

7566802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38360804-C-T

7567282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38361073-C-T

7567288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38361079-T-C

http://identifiers.org/hco/6/GRCh38#7567307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38361108-C-A

7567534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361816-A-G

http://identifiers.org/hco/6/GRCh38#7567536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38361818-C-A

7567537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361819-T-C

7567537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361819-T-G

7567550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361832-A-G

7567566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361848-G-T

7567592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361873-T-C

7567592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361873-T-G

http://identifiers.org/hco/6/GRCh38#7567598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38361879-C-A

7567636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361910-A-G

7567644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361918-A-G

7567688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361962-A-G

http://identifiers.org/hco/6/GRCh38#7567702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38361976-C-A

7567702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38361976-C-T

7567795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38362424-G-A

7567795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38362424-G-T

7567888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38362517-A-G

7567901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38362530-C-G

7567962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362611-C-T

7567965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362612-G-A

7567965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362612-G-T

7568182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362799-T-G

7568194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362811-C-T

7568219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362834-G-A

7568289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362883-T-C

http://identifiers.org/hco/6/GRCh38#7568317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38362911-C-A

7568317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362911-C-T

http://identifiers.org/hco/6/GRCh38#7568387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38362974-A-C

7568387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362974-A-G

7568394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362981-A-G

7568394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38362981-A-T

7568707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38363293-A-G

http://identifiers.org/hco/6/GRCh38#7568738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38363324-C-A

7568738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38363324-C-T

7568820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 38363409-C-T

7569066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365012-G-T

http://identifiers.org/hco/6/GRCh38#7569103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38365048-C-A

7569260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38365148-G-A

7569311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38365199-G-A

7569354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365240-G-T

7569900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365648-A-G

http://identifiers.org/hco/6/GRCh38#7569971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38365732-C-A

7569971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365732-C-T

7569998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365760-A-G

7570189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38365932-C-T

7570251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38366014-A-G

7570321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38366085-A-T

http://identifiers.org/hco/6/GRCh38#7570387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38366150-A-C

7571153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38366891-G-A

7571264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38366993-G-A

7571264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38366993-G-T

http://identifiers.org/hco/6/GRCh38#7571266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38366995-C-A

7571266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38366995-C-T

7571273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367002-G-T

7571314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367028-G-A

http://identifiers.org/hco/6/GRCh38#7571333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38367034-A-C

7571333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367034-A-G

7571333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367034-A-T

7571370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367077-T-A

7571370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367077-T-C

7571371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38367078-G-A

7571400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38367108-G-A

7571520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38367228-C-T

7571745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367835-G-T

7571750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367840-T-C

7571767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367857-T-C

7571767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367857-T-G

7571770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367860-A-T

http://identifiers.org/hco/6/GRCh38#7571783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38367863-C-A

http://identifiers.org/hco/6/GRCh38#7571791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38367871-C-A

http://identifiers.org/hco/6/GRCh38#7571797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38367877-A-C

7571797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38367877-A-G

7571903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38367983-T-C

7571903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38367983-T-G

7571909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38367989-C-G

7571936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38368016-A-G

7571940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38368020-A-G

7571940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38368020-A-T

7572093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368174-T-C

7572127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368207-G-A

7573762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368775-G-A

7573785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368801-A-G

7573807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368818-T-C

7573949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368935-G-A

7573949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368935-G-T

7574000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368974-T-A

7574000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368974-T-C

7574008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368982-G-A

7574008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38368982-G-C

http://identifiers.org/hco/6/GRCh38#7574049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38369032-C-A

7574051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369034-G-A

7574056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369042-A-G

7574072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369058-T-C

http://identifiers.org/hco/6/GRCh38#7574202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38369188-A-C

7574202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38369188-A-G

http://identifiers.org/hco/6/GRCh38#7574235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38369221-A-C

7574235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38369221-A-G

7574270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369256-T-C

7574461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369371-T-A

7574465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369375-C-G

7574476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369383-A-G

7574568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369461-G-T

http://identifiers.org/hco/6/GRCh38#7574660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38369552-A-C

7574738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38369630-G-A

7574786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 38369678-T-A

http://identifiers.org/hco/6/GRCh38#7574811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38369703-A-C

7574811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369703-A-G

7574811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369703-A-T

7574862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38369754-T-C

7574998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38370205-A-T

7575168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38370367-T-A

7575168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38370367-T-G

7575185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38370384-G-A

http://identifiers.org/hco/6/GRCh38#7575209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38370457-C-A

http://identifiers.org/hco/6/GRCh38#7575501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38370777-C-A

7575528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38370799-C-T

7576149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371568-T-C

7576178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371597-T-C

7576235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371657-A-G

7576411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38371834-A-G

7576482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371898-G-A

7576509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371925-T-A

http://identifiers.org/hco/6/GRCh38#7576510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38371926-C-A

7576513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371929-G-T

http://identifiers.org/hco/6/GRCh38#7576590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38371986-C-A

7576590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38371986-C-T

http://identifiers.org/hco/6/GRCh38#7576810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38372304-C-A

7576810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372304-C-T

7576818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372312-T-A

7576823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372317-A-G

http://identifiers.org/hco/6/GRCh38#7576844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38372329-A-C

7576844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372329-A-G

7576849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372334-G-A

7576849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372334-G-C

7576849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372334-G-T

http://identifiers.org/hco/6/GRCh38#7576871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38372352-C-A

7576871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372352-C-T

http://identifiers.org/hco/6/GRCh38#7576924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38372394-C-A

7576924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372394-C-T

7576926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372396-T-C

7576926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372396-T-G

7576931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372401-A-G

7576931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372401-A-T

http://identifiers.org/hco/6/GRCh38#7576945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38372414-C-A

7576945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372414-C-T

7576948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372415-T-C

7576969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38372436-G-A

7577027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38372494-C-T

7577155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372777-G-A

7577155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372777-G-T

7577170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372792-T-A

7577177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372799-A-G

7577253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372893-C-T

7577298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372906-A-T

7577330-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38372938-T-G

7577424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38373032-G-C

http://identifiers.org/hco/6/GRCh38#7577766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38373509-C-A

7577868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38373611-T-C

7577868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38373611-T-G

7577907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38373653-C-T

7577928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38373692-T-C

http://identifiers.org/hco/6/GRCh38#7577938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38373702-C-A

7578092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38373831-T-C

http://identifiers.org/hco/6/GRCh38#7578359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38374170-C-A

7578359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374170-C-T

7578369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374277-A-G

7578369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374277-A-T

http://identifiers.org/hco/6/GRCh38#7578370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38374278-A-C

7578370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374278-A-G

7578481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38374388-T-C

7578526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38374433-C-T

7578539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38374446-C-T

7578544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38374451-G-T

7578593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374506-A-G

7578624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374537-A-G

7578662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374563-G-T

http://identifiers.org/hco/6/GRCh38#7578666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38374567-C-A

http://identifiers.org/hco/6/GRCh38#7578792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38374674-C-A

7578850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38374736-G-A

7579126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375154-G-T

7579151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375195-A-G

7579151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375195-A-T

http://identifiers.org/hco/6/GRCh38#7579155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38375199-A-C

7579155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375199-A-G

7579155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375199-A-T

7579214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38375274-G-T

http://identifiers.org/hco/6/GRCh38#7579529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38375591-A-C

7579529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38375591-A-T

7579571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38375633-T-C

http://identifiers.org/hco/6/GRCh38#7579613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38375675-A-C

7579649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38375711-T-C

7579650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38375712-G-A

7579650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38375712-G-C

7579712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38375774-G-A

7579751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38375813-A-G

7579971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376033-T-C

http://identifiers.org/hco/6/GRCh38#7579979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38376041-C-A

7579979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376041-C-T

http://identifiers.org/hco/6/GRCh38#7579995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38376057-C-A

7579995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376057-C-G

7579995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, stop_gained
orthologous variants: 38376057-C-T

7580000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376062-T-A

7580082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376144-G-A

7580093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376155-G-A

http://identifiers.org/hco/6/GRCh38#7580171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38376233-C-A

7580171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376233-C-G

7580171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376233-C-T

7580177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376239-A-G

7580177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376239-A-T

7580449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376511-C-T

7580660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376722-C-G

7580660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376722-C-T

7580696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 38376758-T-C

7580750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376812-T-A

7580750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376812-T-G

7580754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376816-A-T

7580767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38376829-A-G

7580918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38376980-G-A

7580927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 38376989-G-A

7580981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 38377043-G-A

7580981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 38377043-G-T

http://identifiers.org/hco/6/GRCh38#7581119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38377181-C-A

7581158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38377220-G-A

7581158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, missense_variant
orthologous variants: 38377220-G-C

http://identifiers.org/hco/6/GRCh38#7581173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38377235-C-A

7581173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38377235-C-G

7581173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38377235-C-T

http://identifiers.org/hco/6/GRCh38#7581610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38377672-A-C

7581645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38377703-C-T

7582273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378304-A-G

7582471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378507-C-G

7582471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378507-C-T

7582507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378534-G-A

7582507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378534-G-T

7582522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378549-A-G

http://identifiers.org/hco/6/GRCh38#7582559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38378579-C-A

7582559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378579-C-G

7582582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378605-T-C

7582616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: intron variant
orthologous variants: 38378641-C-G

7582794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38378824-G-A

7582794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38378824-G-T

7582875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: stop gained
orthologous variants: 38378905-T-G

7582959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38378989-C-G

7582959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38378989-C-T

7583103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379133-T-C

7583106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379136-G-A

7583106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379136-G-C

7583156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38379186-A-G

7583187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379217-G-A

7583214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379244-G-A

7583465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38379495-C-G

7583610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38379640-T-G

7583652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379682-T-C

http://identifiers.org/hco/6/GRCh38#7583838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38379868-C-A

7583838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379868-C-T

7583910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379940-T-G

7583952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38379982-G-A

http://identifiers.org/hco/6/GRCh38#7583994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38380024-C-A

7583994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380024-C-G

7583994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38380024-C-T

7584066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38380096-A-G

7584123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38380153-T-G

7584303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380333-C-G

7584303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38380333-C-T

http://identifiers.org/hco/6/GRCh38#7584655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38380685-A-C

7584655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380685-A-G

7584659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380689-T-C

http://identifiers.org/hco/6/GRCh38#7584817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38380847-C-A

7584817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38380847-C-T

http://identifiers.org/hco/6/GRCh38#7584834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38380864-A-C

7584905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380935-G-A

7584905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: missense variant
orthologous variants: 38380935-G-C

7585110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381140-G-A

7585110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381140-G-C

7585200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381230-G-A

7585200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381230-G-C

7585401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381431-G-A

7585401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381431-G-C

7585416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381446-C-G

7585716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: synonymous variant
orthologous variants: 38381746-C-T

7585880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38381910-A-G

7585992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382008-G-A

7586017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382029-G-T

7586168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382158-G-A

7586168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382158-G-T

http://identifiers.org/hco/6/GRCh38#7586331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38382318-C-A

7586331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382318-C-T

7586362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382331-G-A

7586362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382331-G-T

7586610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: 38382589-G-T

http://identifiers.org/hco/6/GRCh38#7586687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3052
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38382671-A-C