18080942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139469984-A-G

18080942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139469984-A-T

18080973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470012-T-C

18080996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470035-G-A

18080996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470035-G-T

18081087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470123-G-T

http://identifiers.org/hco/12/GRCh38#18081108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139470131-A-C

18081108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470131-A-G

18081108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470131-A-T

18081122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470144-G-A

18081122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470144-G-T

18081149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470171-G-C

18081149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139470171-G-T

18081259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139470280-G-A

18081372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139470393-C-T

18081373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139470394-G-A

18081436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139470457-G-A

http://identifiers.org/hco/12/GRCh38#18081467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139470488-C-A

18081467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139470488-C-T

18081505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470524-T-A

18081505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470524-T-C

18081505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470524-T-G

18081560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470570-G-A

18081560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470570-G-T

18081607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470620-G-T

18081739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139470745-C-T

18083885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471191-G-A

18083906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471212-A-G

18084032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471331-T-C

18084032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471331-T-G

18084399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471698-T-C

18084399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471698-T-G

18084632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139471931-G-A

18084632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139471931-G-T

18084656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139471955-C-G

18084694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139471991-G-T

18084707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472004-A-T

18084708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472005-C-G

18084708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472005-C-T

18084710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472007-T-A

18084710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472007-T-C

18084734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472022-A-T

18084749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472037-A-G

18084749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472037-A-T

18084768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472043-T-C

18084959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139472205-G-T

http://identifiers.org/hco/12/GRCh38#18085732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139473578-C-A

18085732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473578-C-T

18085740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473609-G-A

18085740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473609-G-C

18085740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473609-G-T

18085744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473613-A-G

18085744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473613-A-T

http://identifiers.org/hco/12/GRCh38#18085790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139473644-C-A

18085790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139473644-C-T

http://identifiers.org/hco/12/GRCh38#18086508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139474327-A-C

http://identifiers.org/hco/12/GRCh38#18086512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139474331-A-C

18086512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139474331-A-G

18086621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139474445-T-A

18086927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139474724-T-A

18086929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139474726-G-C

18086945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139474742-A-G

18087294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476026-G-C

18087296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476028-T-C

18087431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476170-T-C

18087626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476363-T-C

18087709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476446-G-A

18087737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476481-T-C

18087804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476554-T-C

18087830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476580-T-A

18087908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476659-G-A

18088017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476767-C-T

18088043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476789-T-G

18088186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476915-T-A

18088248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139476970-G-T

18088592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477367-C-T

http://identifiers.org/hco/12/GRCh38#18088597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139477372-C-A

18088782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477579-A-G

http://identifiers.org/hco/12/GRCh38#18088816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139477611-A-C

18088844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477639-G-T

18088928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139477747-T-A

18088984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477804-G-A

18088984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477804-G-T

http://identifiers.org/hco/12/GRCh38#18089083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139477900-C-A

18089083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477900-C-T

18089092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477909-G-A

18089092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477909-G-C

18089092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477909-G-T

18089093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477910-T-C

18089158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477959-G-A

18089158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477959-G-C

18089158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477959-G-T

18089170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477970-C-T

18089183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477983-T-A

18089183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139477983-T-C

18089201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478000-A-G

18089216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478015-T-A

18089216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478015-T-C

18089216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478015-T-G

18089365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139478161-G-A

18089365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139478161-G-T

18089379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139478175-T-C

http://identifiers.org/hco/12/GRCh38#18089413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139478206-C-A

18089413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478206-C-G

18089477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478263-T-C

18089480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478266-G-A

18089480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478266-G-T

18089586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478369-C-G

18089586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478369-C-T

18089591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478374-T-C

18089593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478376-C-T

18089601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478384-T-C

18089640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478426-G-A

18089640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478426-G-C

18089691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478471-C-G

18089738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478514-A-G

18089949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478723-T-A

18089949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478723-T-C

http://identifiers.org/hco/12/GRCh38#18089953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139478727-C-A

18089953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478727-C-T

18089959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478733-G-A

18089959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478733-G-C

18089959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478733-G-T

http://identifiers.org/hco/12/GRCh38#18090056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139478791-C-A

18090056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478791-C-T

18090170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478904-T-A

18090170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478904-T-C

18090175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478909-T-C

18090179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478913-A-G

http://identifiers.org/hco/12/GRCh38#18090180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139478914-C-A

18090180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478914-C-G

18090180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478914-C-T

18090183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139478917-C-T

18090223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478955-T-C

18090231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139478963-T-C

18090283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139479021-T-C

18090567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139479242-T-C

http://identifiers.org/hco/12/GRCh38#18104752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139484190-A-C

18104990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139485546-G-T

18104997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139485553-G-T

18105026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139485585-C-T

18105100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139485663-G-A

18105162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139485718-T-C

18110282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139486951-T-C

18110302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139486971-T-C

http://identifiers.org/hco/12/GRCh38#18113014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139487922-A-C

18113142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139488038-C-T

18114272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139489241-G-C

18114633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139489579-A-G

18114634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139489580-C-T

18114857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139489825-A-G

18114936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139489900-A-G

http://identifiers.org/hco/12/GRCh38#18115003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139489960-C-A

18115126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490079-C-T

18115431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490312-T-C

18115478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490360-G-T

18115555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490435-A-T

18115914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490790-G-A

18115915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490791-G-T

18115950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490828-A-G

18115950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139490828-A-T

18116668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139492848-G-A

18116668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139492848-G-T

18116731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139492909-G-C

18119507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139494820-T-C

18119606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139494914-G-C

18119690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139494999-T-C

18126091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139497854-T-A

18126091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139497854-T-C

18126106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139497866-T-C

18126109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139497869-C-T

18126170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139497932-T-C

18129360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139499529-A-G

18129433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139499601-A-G

http://identifiers.org/hco/12/GRCh38#18129742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139500217-C-A

18129906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139500372-C-G

18129934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139500387-T-C

18130249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139500698-T-C

18130593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501094-A-G

18130648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501154-T-G

18130713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501219-G-C

http://identifiers.org/hco/12/GRCh38#18131204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139501682-A-C

http://identifiers.org/hco/12/GRCh38#18131222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139501700-A-C

18131222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501700-A-T

18131245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501723-T-C

18131261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501739-A-G

18131311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139501790-T-A

http://identifiers.org/hco/12/GRCh38#18131378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139501876-A-C

http://identifiers.org/hco/12/GRCh38#18131513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139502004-C-A

18131738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139502226-A-G

18131852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139502330-C-T

http://identifiers.org/hco/12/GRCh38#18133051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139503458-C-A

18133051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139503458-C-T

http://identifiers.org/hco/12/GRCh38#18133215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139503604-A-C

18133263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139503672-T-C

18133952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504243-G-C

http://identifiers.org/hco/12/GRCh38#18133968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139504259-C-A

18134146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504477-G-C

18134157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504489-T-A

18134157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504489-T-G

18134278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504610-A-G

18134495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504831-G-A

18134495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504831-G-T

18134511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139504847-A-G

18136032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505413-T-C

18136090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505466-A-G

18136399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505679-G-A

18136407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505687-G-A

18136544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505867-G-A

18136649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139505944-T-C

18137189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139507335-C-G

18137189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139507335-C-T

18138031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513313-C-T

18138238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513504-T-C

18138238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513504-T-G

18138580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513762-T-A

18138589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513771-C-T

18138599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513775-C-G

18138656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139513819-G-C

18139036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139514217-T-G

18139064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139514408-A-G

18139176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139514513-G-A

18139368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139514713-A-G

18139572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139514876-A-G

18139751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139515045-G-T

18139754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139515048-T-G

18139817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139515116-G-A

http://identifiers.org/hco/12/GRCh38#18139953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139515295-A-C

18140262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139515764-T-A

18140299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139515801-G-A

http://identifiers.org/hco/12/GRCh38#18167310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139523240-C-A

18167310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139523240-C-T

18167816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139523438-A-T

18167966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139523587-C-T

18167979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139523601-T-A

18168085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139523705-A-G

18168387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139524186-T-C

18168592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139524384-G-A

18168592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139524384-G-C

18168949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139525635-C-T

18169039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139525707-A-G

18204378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139532715-A-G

18204405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139532736-A-G

18204423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139532754-A-G

18204694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139533014-G-A

18204716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139533036-G-T

18205162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139533462-C-G

18205304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139533581-T-C

18205425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139533687-A-G

18206005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139535412-G-C

18206012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139535419-G-A

18206223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139535631-G-C

18206227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139535635-A-G

18206901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139536021-T-G

18206914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139536034-G-T

18209546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139537751-T-C

http://identifiers.org/hco/12/GRCh38#18209773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139539694-A-C

18209773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139539694-A-T

18209825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139539733-G-A

18209929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139539832-T-C

http://identifiers.org/hco/12/GRCh38#18209975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139539878-C-A

18209975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139539878-C-T

18210030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139539933-C-T

http://identifiers.org/hco/12/GRCh38#18210071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139539973-C-A

18210286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540185-A-G

18210365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540267-T-C

18210409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540297-T-C

18210409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540297-T-G

18210422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540312-A-G

18210512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540401-G-A

18210584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540468-G-A

18210584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540468-G-C

18210687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540567-T-C

18210824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540685-G-C

18210840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540701-A-G

18210853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540715-T-C

18210856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540718-G-A

18210889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139540750-C-T

18216378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544049-C-T

18216412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544082-A-T

18216455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544108-T-A

18216463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544116-G-T

18216502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544567-G-A

18216512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544577-G-A

18216524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544590-C-T

18216620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544682-T-A

18216620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544682-T-C

18216679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544744-C-G

http://identifiers.org/hco/12/GRCh38#18216692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139544754-C-A

18216692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544754-C-G

18216734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544791-C-G

18216735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139544792-A-T

18217305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139545232-G-A

18217305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139545232-G-T

18217523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139545654-T-C

18217891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546159-G-A

18217891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546159-G-T

18217987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546258-C-G

18218019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546283-T-C

18218123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546386-A-G

18218254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546504-T-A

18218316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546560-T-A

http://identifiers.org/hco/12/GRCh38#18218457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139546691-A-C

18218459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546693-A-G

18218460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546694-C-T

18218661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546817-A-G

18218746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546881-T-A

18218775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546910-C-T

18218820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139546958-C-T

18219092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547208-T-C

18219110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547226-G-T

18219292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547277-A-G

18219312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547293-A-G

http://identifiers.org/hco/12/GRCh38#18219344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139547314-A-C

18219344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547314-A-G

18219631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547561-T-C

18219724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547657-A-G

18219794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547733-T-C

18219899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547830-A-G

18219913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547844-A-G

18220094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139547993-T-C

18220479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548202-T-C

18220876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548635-T-C

18221028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548913-T-C

http://identifiers.org/hco/12/GRCh38#18221046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139548932-A-C

18221074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548958-C-G

18221085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548969-A-G

18221086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139548984-G-C

18221239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549108-T-C

18221303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549170-G-A

18221588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549474-G-C

18221611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549495-G-T

http://identifiers.org/hco/12/GRCh38#18221739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139549609-A-C

18221741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549611-A-G

18221867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139549732-C-T

18222477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139550331-G-A

18222477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139550331-G-C

18222701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139550536-T-G

18223599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553643-G-A

18223599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553643-G-C

18223794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553813-T-A

18223853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553867-A-G

18223885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553896-T-A

18223904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553913-C-G

18223926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553937-G-C

18223933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553944-G-A

18223955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139553967-T-C

http://identifiers.org/hco/12/GRCh38#18224054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139554056-A-C

18224174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554169-G-A

18224194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554191-C-T

18224205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554201-G-A

18224398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554378-T-C

http://identifiers.org/hco/12/GRCh38#18224415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139554395-A-C

http://identifiers.org/hco/12/GRCh38#18224871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139554596-A-C

18224892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554618-C-T

18225031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554759-C-G

http://identifiers.org/hco/12/GRCh38#18225290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139554972-A-C

http://identifiers.org/hco/12/GRCh38#18225297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139554980-C-A

18225297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139554980-C-G

18225439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139555101-A-G

18225915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139555527-G-T

18239578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139558773-G-A

18239688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139558902-A-G

18239810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139559020-T-C

18239858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139559068-G-T

18240043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139559580-T-C

18240045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139559582-G-A

18241708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139562971-A-G

18241763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563026-T-G

18241779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563042-T-C

18241779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563042-T-G

18242005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563262-T-G

http://identifiers.org/hco/12/GRCh38#18242039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139563296-A-C

http://identifiers.org/hco/12/GRCh38#18242171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139563438-A-C

18242249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563510-T-G

18242294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563555-T-A

18242375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563631-A-G

18242405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139563676-C-T

http://identifiers.org/hco/12/GRCh38#18242462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139563747-A-C

18242773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139563984-C-G

18242819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139564029-T-C

18242885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564106-C-G

18242965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139564180-A-G

http://identifiers.org/hco/12/GRCh38#18243068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139564268-A-C

18243108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564304-T-A

http://identifiers.org/hco/12/GRCh38#18243190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139564393-C-A

18243210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564408-G-A

18243211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564409-T-C

18243255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564453-T-A

18243385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564518-G-A

18243427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564548-G-T

18243453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564572-T-A

18243453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564572-T-C

18243597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564706-T-G

18243751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564856-A-T

18243768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564873-T-C

18243830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139564925-T-C

18250059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566266-A-G

18250441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566420-T-C

18250468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566445-G-A

18250544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566514-C-T

18250551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566521-A-T

18250581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566550-C-T

18250602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566574-G-C

18250699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566661-T-G

18250795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566758-A-G

18250816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566785-T-C

18250931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139566884-A-G

18256104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139569691-T-C

18256113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139569700-C-T

18256130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139569717-A-G

http://identifiers.org/hco/12/GRCh38#18256147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139569734-A-C

http://identifiers.org/hco/12/GRCh38#18256396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139569964-C-A

18256415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139569983-C-T

18256492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139570059-C-G

18256492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139570059-C-T

18258821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139571733-G-A

18258823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139571735-C-T

18258929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139571851-T-C

18258937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139571859-A-G

http://identifiers.org/hco/12/GRCh38#18259088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139572008-C-A

18259092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572012-G-A

18259106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572026-A-G

18259175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572101-C-G

18259188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572114-T-A

18259268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572191-G-A

18259397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572324-G-C

18259415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572331-G-A

http://identifiers.org/hco/12/GRCh38#18259453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139572367-C-A

18259459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572370-G-A

18259518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572386-A-G

18259558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572424-G-A

18259696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572562-A-G

18259704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139572570-C-T

18260044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139574722-G-C

18260046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139574724-A-G

18260066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139574743-G-T

http://identifiers.org/hco/12/GRCh38#18260605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139575766-C-A

18260623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139575784-C-T

18260665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139575826-T-A

18260719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139575872-G-A

http://identifiers.org/hco/12/GRCh38#18260912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139575987-C-A

18260925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139575999-T-C

18261082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139576122-G-A

18261203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139576202-T-G

18261204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139576203-T-A

18261246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139576246-T-A

18261367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139576364-G-A

18261474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139576461-G-A

18261782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576713-G-A

18261785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576716-A-G

18261800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576741-A-T

18261826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576791-C-G

18261846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576811-C-G

18261896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576857-A-G

18261903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576871-C-T

18262025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139576988-G-A

18262325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577260-A-G

http://identifiers.org/hco/12/GRCh38#18262333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139577266-C-A

18262485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577403-C-T

18262584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577518-T-A

http://identifiers.org/hco/12/GRCh38#18262595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139577577-C-A

18262595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577577-C-T

18262606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577588-T-A

18262606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577588-T-G

http://identifiers.org/hco/12/GRCh38#18262632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139577656-C-A

18262632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577656-C-G

18262739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577763-C-G

18262766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 139577788-T-C

18262820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139577839-A-G

18263197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578474-G-A

18263289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578550-T-C

18263317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578575-T-C

http://identifiers.org/hco/12/GRCh38#18263476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139578725-C-A

18263476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578725-C-T

18263486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578735-G-A

18263497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139578746-T-C

18263842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139579150-C-G

18267745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587216-T-C

18267802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587271-C-T

18267915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587376-G-A

18268035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587473-T-C

18268082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587511-C-G

18268082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587511-C-T

18268096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587525-T-C

http://identifiers.org/hco/12/GRCh38#18268129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139587551-A-C

18268154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587586-G-A

18268154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587586-G-C

18268241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139587733-G-A

18269383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588258-A-G

18269457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588324-C-T

18269471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588338-A-T

18269697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588534-T-C

18270318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588927-C-T

18270342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139588951-A-T

18270441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589041-T-C

18270441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589041-T-G

http://identifiers.org/hco/12/GRCh38#18270486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139589085-A-C

http://identifiers.org/hco/12/GRCh38#18270736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139589502-A-C

18270736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589502-A-G

18270759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589525-C-T

18270770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589536-T-C

18270932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589672-G-T

18271102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589824-T-G

18271153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139589867-C-T

http://identifiers.org/hco/12/GRCh38#18275695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139591878-C-A

http://identifiers.org/hco/12/GRCh38#18275943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139592077-C-A

18275984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592119-T-A

18276026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139592152-A-G

18276030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139592156-G-A

18276184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139592287-C-T

18276324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139592420-G-A

18276536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592593-A-G

18276648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592673-C-T

18276731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592751-G-A

http://identifiers.org/hco/12/GRCh38#18276990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139592983-C-A

18276990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592983-C-G

18277009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139592997-A-G

18277249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593221-T-C

18277278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593247-T-C

18277337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593276-G-C

18277344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593283-G-A

18277397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593337-G-A

18277428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593364-T-C

18277582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593520-T-C

18277798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593737-G-A

18277849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593783-A-G

18277849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139593783-A-T

18281769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598588-C-T

http://identifiers.org/hco/12/GRCh38#18281784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139598607-C-A

18281784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598607-C-G

18281898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598705-A-G

18281903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598710-G-A

18281903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598710-G-C

18281903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598710-G-T

http://identifiers.org/hco/12/GRCh38#18281913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139598717-C-A

18281913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598717-C-T

18281956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598759-T-C

18281973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139598776-T-C

http://identifiers.org/hco/12/GRCh38#18282026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#139598832-A-C

18282026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139598832-A-G

18282026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139598832-A-T

18282162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139598966-A-G

http://identifiers.org/hco/12/GRCh38#18282183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139598987-C-A

18282231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599035-A-T

18282296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599100-A-T

18282334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599138-T-G

18282370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599174-T-C

18282370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599174-T-G

18282410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599214-G-A

18282442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599246-A-G

18282470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599274-T-C

18282479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599283-A-G

18282514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599318-G-A

18282537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139599341-T-C

18282587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599391-T-A

18282587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599391-T-C

18282614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599417-C-T

18282633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599437-T-G

18282644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599448-C-T

18282645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139599449-G-A

18282718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599522-C-G

18282718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 139599522-C-T

18282732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599536-G-C

18282732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599536-G-T

18282790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599586-T-C

http://identifiers.org/hco/12/GRCh38#18282809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139599600-C-A

18282809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599600-C-T

18282859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599649-G-A

18282859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599649-G-T

18282868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599658-T-C

18282868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599658-T-G

18282985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599759-C-T

http://identifiers.org/hco/12/GRCh38#18283037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139599848-C-A

18283184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139599989-G-A

http://identifiers.org/hco/12/GRCh38#18283298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139600103-C-A

18283353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139600163-A-G

18283563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139600943-A-T

18283605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139600978-C-G

18283645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139601664-G-A

18283645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139601664-G-T

18286023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139602725-G-A

http://identifiers.org/hco/12/GRCh38#18286092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139602789-C-A

18286092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139602789-C-T

18286242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139602918-T-C

18286348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603018-G-A

18286348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603018-G-T

18286689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603343-T-C

18286714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603368-C-T

http://identifiers.org/hco/12/GRCh38#18286755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139603400-C-A

18286849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 139603496-A-G

18286870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost, synonymous_variant, undefined
orthologous variants: 139603517-A-G

18286870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost, synonymous_variant, undefined
orthologous variants: 139603517-A-T

http://identifiers.org/hco/12/GRCh38#18286937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139603584-C-A

18286937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 139603584-C-T

18286938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603585-T-A

18286938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603585-T-C

18286938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603585-T-G

18286939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603586-G-A

18286939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603586-G-T

18286966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603613-G-T

18286972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603619-G-A

18286972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603619-G-T

18287000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603647-G-T

18287032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603680-T-C

18287037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603684-T-C

18287182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603817-T-C

18287253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603885-C-G

18287269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139603901-A-G

18287381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604005-C-T

18287404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604017-T-C

18287404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604017-T-G

18288500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604497-G-A

http://identifiers.org/hco/12/GRCh38#18288861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139604943-C-A

18288861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604943-C-T

18288898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139604978-G-A

18289090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139605224-T-C

18289116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139605240-A-G

18289410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139605548-T-C

18289674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139605732-G-A

http://identifiers.org/hco/12/GRCh38#18289841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139605844-A-C

18289877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139605870-A-G

http://identifiers.org/hco/12/GRCh38#18289884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139605877-A-C

18290116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606099-T-C

18290237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606189-C-T

18290397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606282-T-C

18290579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606454-T-C

18290585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606460-A-G

18290680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606551-T-G

18290698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606569-A-T

18290756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606621-A-G

18290821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606675-G-A

18290821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606675-G-C

18290821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606675-G-T

http://identifiers.org/hco/12/GRCh38#18290824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139606678-C-A

18290824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606678-C-G

18290824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606678-C-T

18290915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139606776-T-C

18290954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139606815-G-A

18290954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606815-G-C

http://identifiers.org/hco/12/GRCh38#18290986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139606847-C-A

18290986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606847-C-T

18290987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139606848-A-G

18290996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139606857-T-C

18291011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, stop_gained, undefined
orthologous variants: 139606872-T-A

18291011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 139606872-T-C

18291055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606898-G-A

18291055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139606898-G-T

18291209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607026-T-A

18291209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607026-T-C

18291226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607043-C-T

18291418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607214-C-T

18291456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607252-G-A

18291476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607271-G-A

18291543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607337-C-T

18291560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607352-T-C

18292257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607696-G-A

18292257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607696-G-T

18292412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607844-C-T

18292458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139607911-A-G

18292614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139608042-T-C

18292654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139608075-A-G

http://identifiers.org/hco/12/GRCh38#18293152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139609658-A-C

18293277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139609778-G-A

18293322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139609823-A-G

18293332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139609833-T-C

18293656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139610429-T-C

18293670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139610443-A-G

http://identifiers.org/hco/12/GRCh38#18293821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139610595-C-A

http://identifiers.org/hco/12/GRCh38#18293963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139610737-C-A

18294103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139610881-C-T

http://identifiers.org/hco/12/GRCh38#18294789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139613241-A-C

18294789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139613241-A-G

18294797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139613249-C-T

18294871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139613323-C-T

18296918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618026-C-T

18297021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618126-T-C

18297139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618246-C-T

18303746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618564-C-T

18303872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618671-T-C

18304130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139618922-C-T

18304603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139619937-T-C

18304686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620014-T-C

18305405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620563-G-A

http://identifiers.org/hco/12/GRCh38#18305413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139620571-A-C

http://identifiers.org/hco/12/GRCh38#18305488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139620642-C-A

18305507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620661-T-C

18305517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620671-A-G

18305532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620682-C-T

18305649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620795-C-T

18305723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620869-G-T

18305779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139620920-C-T

18306108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139621213-A-T

18306280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139621373-G-T

18306421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139621510-G-C

18306421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139621510-G-T

18306462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139621553-C-T

18306798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139622014-T-A

18306840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139622062-A-G

18306973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139622819-C-T

http://identifiers.org/hco/12/GRCh38#18307162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139623004-C-A

18307199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623042-A-T

18307365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623205-G-A

18307402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623246-A-G

18307442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623284-G-T

18307536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623352-G-A

18307543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623359-T-C

18307553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623369-A-G

18307689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623502-C-G

18307732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139623544-C-T

http://identifiers.org/hco/12/GRCh38#18313831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139625978-C-A

18313831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625978-C-G

18313831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625978-C-T

http://identifiers.org/hco/12/GRCh38#18313835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139625982-C-A

18313835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625982-C-T

http://identifiers.org/hco/12/GRCh38#18313837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139625984-C-A

18313837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625984-C-G

18313837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625984-C-T

18313840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625987-G-A

18313840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139625987-G-T

18313848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626007-T-A

18313848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626007-T-G

http://identifiers.org/hco/12/GRCh38#18313905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626063-C-A

18313905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626063-C-T

18313906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626064-A-G

18313906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626064-A-T

18313916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626073-G-A

18313916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626073-G-T

18313940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626104-T-C

18313941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626105-G-A

18313941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626105-G-T

http://identifiers.org/hco/12/GRCh38#18313945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626109-A-C

18313945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626109-A-G

18313945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626109-A-T

18313951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626116-T-C

18313951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626116-T-G

http://identifiers.org/hco/12/GRCh38#18313953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626118-C-A

18313953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626118-C-G

18313953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626118-C-T

18313978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626143-A-G

18313978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626143-A-T

18314033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626198-G-A

18314033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626198-G-T

http://identifiers.org/hco/12/GRCh38#18314039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626204-A-C

18314047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626212-G-A

18314047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 139626212-G-T

18314085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626250-G-A

18314085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626250-G-T

18314128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626294-T-C

18314175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626342-G-T

http://identifiers.org/hco/12/GRCh38#18314192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626359-C-A

18314201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626368-A-G

18314203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626370-G-A

18314383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626548-G-T

18314389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626554-G-T

18314403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626567-G-C

18314403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626567-G-T

18314427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626585-C-T

18314502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626615-T-C

http://identifiers.org/hco/12/GRCh38#18314511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139626624-C-A

18314511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626624-C-T

18314524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 139626637-A-G

18314525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 139626638-G-A

18314525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 139626638-G-T

18314530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626643-G-T

18314531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 139626644-G-A

18314531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626644-G-C

18314544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626657-G-A

18314568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626681-G-A

18314568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626681-G-T

18314592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626705-T-C

18314629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139626718-G-T

18314968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627082-T-G

18315021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627134-A-G

18315139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627264-T-C

18315143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627268-T-A

18315197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627382-G-A

18315270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139627454-G-A

18318448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139631224-A-G

18319155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139631529-A-G

18319732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632616-T-A

18319757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632645-C-T

18319762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632650-C-T

18319841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632710-C-T

18319932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632758-A-G

18319932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632758-A-T

18319967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632798-T-C

18319982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632813-G-T

http://identifiers.org/hco/12/GRCh38#18320003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#139632834-C-A

18320003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632834-C-G

18320101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632925-T-A

18320101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 139632925-T-C