37907296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29217950-G-T

37907309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29217937-C-T

37907403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217843-G-A

37907403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217843-G-T

37907409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217837-C-T

37907468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29217765-C-T

37907517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29217716-T-C

37907558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29217675-G-A

37907558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29217675-G-T

http://identifiers.org/hco/19/GRCh38#37907580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29217653-C-A

37907580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29217653-C-T

37907662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29217571-G-T

37908160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29217053-A-G

37908675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, undefined
orthologous variants: 29216579-C-T

37909139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29216099-G-A

37909546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29215833-A-G

37909728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29215657-G-A

37909936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29215453-A-G

37910274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29215095-A-G

37910990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29214821-T-C

37911015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29214796-C-T

37911140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29214674-T-C

http://identifiers.org/hco/19/GRCh38#37911210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29214609-C-A

37911319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29214521-G-C

37912919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29214118-C-T

37913058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29213994-C-T

37913084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29213972-A-G

37913211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29213842-G-A

37913234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29213815-T-C

37913292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29213757-G-T

37914980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29212969-C-T

37920605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29211387-G-A

37921028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29211022-G-C

37921077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29210972-T-C

37921208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29210848-C-G

37921413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29210640-G-C

37926090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208576-G-A

37926100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208566-A-G

37926123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208545-A-G

37926149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208519-T-C

http://identifiers.org/hco/19/GRCh38#37926325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29208347-C-A

37926365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208318-G-T

37926665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208132-G-A

37926781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29208032-C-T

37926877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29207942-G-A

37926877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29207942-G-C

37928864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29207587-A-G

37929017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, undefined
orthologous variants: 29207471-A-G

37929140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29207360-G-C

37931981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29205330-C-T

37932074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29205286-C-T

37932232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29205142-A-G

37932401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29204995-G-T

37932501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 29204902-A-G

http://identifiers.org/hco/19/GRCh38#37932511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#29204892-C-A

37932962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204393-G-A

37932998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204360-C-G

37933028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204332-C-G

37933028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29204332-C-T

http://identifiers.org/hco/19/GRCh38#37933149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29204200-A-C

37933537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29203928-G-A

37933537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29203928-G-C

37933684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29203766-A-G

37933756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203688-G-A

37933767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203677-A-G

37933808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203635-C-T

37933991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203480-T-C

37934083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203390-G-A

37934083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203390-G-T

37934098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29203375-G-A

http://identifiers.org/hco/19/GRCh38#37934290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29203178-C-A

http://identifiers.org/hco/19/GRCh38#37934615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29202896-C-A

37934909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201891-G-A

37934980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201830-T-C

37935300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201509-T-G

37935503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29201350-A-G

http://identifiers.org/hco/19/GRCh38#37935531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29201322-C-A

37935955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29200792-G-A

37936320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29200499-A-T

37936386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29200432-A-T

http://identifiers.org/hco/19/GRCh38#37936608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29200223-A-C

37936608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29200223-A-G

37940824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196945-C-T

37940902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196896-C-T

37940914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196884-A-G

37941178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196634-C-T

37941218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196599-G-T

37941474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196365-G-T

37941583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196279-C-T

37941606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196257-G-T

37941632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196231-G-A

37941636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196227-G-A

37941660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196187-G-A

37941694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196150-T-C

37941719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196135-A-G

37941723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29196131-T-C

37941896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195961-G-A

37941983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195875-T-C

37942000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195858-C-G

37942000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195858-C-T

37942019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195839-T-C

37942525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195448-G-A

37942575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29195407-A-G

37943079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29194879-G-T

37943312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29194707-G-T

37947725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192603-A-G

http://identifiers.org/hco/19/GRCh38#37947770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29192561-A-C

37947982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29192345-G-T

37951361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29191379-T-C

37951943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190711-C-T

37952635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190315-T-G

37952747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190262-C-T

37952919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190099-T-A

37952919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190099-T-C

37952972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29190043-C-T

37953019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189996-C-T

37953020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189995-G-A

37953266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189766-C-T

37953286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189747-A-G

http://identifiers.org/hco/19/GRCh38#37953292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29189741-C-A

37953292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189741-C-T

http://identifiers.org/hco/19/GRCh38#37953403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29189632-A-C

37953535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29189566-T-C

37953695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189415-C-T

37953744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29189377-G-A

37953912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189223-C-T

37954023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29189120-A-G

37954509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29188470-C-G

37965340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184602-G-A

37965340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184602-G-T

http://identifiers.org/hco/19/GRCh38#37965371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29184536-A-C

37965371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184536-A-G

37965503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184412-A-G

http://identifiers.org/hco/19/GRCh38#37965514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29184372-C-A

37965890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184116-C-T

37965965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184071-A-G

37966024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184012-G-A

37966024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29184012-G-T

37966321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29183766-G-A

37966342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29183745-G-T

37966583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29183530-T-C

37966766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29183354-G-T

37967075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29183034-G-A

37967283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29182847-T-C

37968888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181410-G-A

37969008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181292-G-A

37969149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181244-A-G

37969265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181211-T-A

37969466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181094-T-C

http://identifiers.org/hco/19/GRCh38#37969617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29181064-C-A

37969617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181064-C-T

37969644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29181042-C-T

37969853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180848-T-C

37969853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180848-T-G

37970244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180478-G-A

37970300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180424-G-C

37970635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180171-C-T

37970739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180104-A-T

37970756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29180086-A-G

37973611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176963-T-G

37973648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176924-T-G

37973651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176921-C-T

37973679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29176893-C-T

37973928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176636-G-A

37974083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29176491-T-G

http://identifiers.org/hco/19/GRCh38#37974517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29176278-A-C

37974776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175344-A-G

37974883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175222-G-A

37974883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175222-G-T

37974997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175157-G-A

http://identifiers.org/hco/19/GRCh38#37975022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29175144-A-C

37975078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29175090-A-G

37976283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29173949-T-C

37976299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29173933-G-C

37976467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29173818-A-G

37976711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29173595-G-A

37977706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172541-C-T

37978182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172094-C-T

37978197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29172079-C-T

37978238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29172040-C-T

37978399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171954-C-T

37978471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171895-A-G

37979728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29171129-T-C

37979901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170967-T-G

37980378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170544-C-T

37980407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170517-C-G

37980869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170214-T-C

37980940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170144-G-A

37980995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29170091-A-G

37981407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169865-A-G

37981409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169863-G-T

37981418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169854-G-A

37981418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169854-G-T

37981494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169770-G-A

37981536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169740-C-T

37981711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169485-A-G

37981860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29169369-A-T

37981970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169258-C-T

37982005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29169225-A-G

37982392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168875-C-G

http://identifiers.org/hco/19/GRCh38#37982429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29168840-C-A

37982515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168834-G-A

37983012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29168331-G-A

http://identifiers.org/hco/19/GRCh38#37983452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29167955-C-A

37983551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167868-T-C

37984070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29167670-G-A

37985946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165707-C-T

37985978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165688-G-A

37986197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165564-A-G

37986250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29165519-C-G

37986250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29165519-C-T

37986671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165154-C-G

37986671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165154-C-T

37986722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165104-C-T

37986756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29165066-G-A

37987649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29164632-T-A

37987783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29164530-T-C

http://identifiers.org/hco/19/GRCh38#37987852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29164501-A-C

37987852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29164501-A-G

37989876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163880-T-G

37990069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29163681-G-A

37990078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163673-T-A

37990143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163602-T-A

37990365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163423-G-A

37990684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163128-T-C

37990687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163125-A-G

37990692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163120-T-C

37990777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29163039-T-C

37991293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162670-G-C

37991390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162594-C-T

37991526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162494-A-G

37991536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162486-T-G

37991565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162458-G-C

37991566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162457-C-T

37991652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162410-G-A

37991898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29162176-A-T

37992042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29162046-T-A

http://identifiers.org/hco/19/GRCh38#37992175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29161895-C-A

37992179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161890-C-T

37992298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161820-A-G

37992299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161819-C-T

37994256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161473-T-C

37994300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161430-G-A

37994603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29161129-G-T

http://identifiers.org/hco/19/GRCh38#37994873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29160865-C-A

37994873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160865-C-T

37994948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160821-A-G

37995067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160763-G-C

37995234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160648-G-A

37995234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160648-G-T

37995448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160100-T-C

37995498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160046-G-A

37995498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29160046-G-C

37995578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159971-A-G

37995585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159964-T-G

37995602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159930-G-A

37995651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159876-G-C

37995655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159872-G-C

37995691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159831-G-A

37995711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29159812-G-A

37998261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158641-T-C

37998655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158236-G-C

37998850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29158085-G-T

37998944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157999-T-G

37999037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157954-T-C

37999386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157679-A-G

37999478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157619-T-C

37999492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157603-A-G

37999533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29157559-T-A

http://identifiers.org/hco/19/GRCh38#37999680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29157409-C-A

38001945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155539-T-C

38002051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155438-A-G

38002214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29155266-A-G

38003880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29152695-T-C

38004217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29152284-G-A

38004648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151869-G-A

38004839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151647-C-T

http://identifiers.org/hco/19/GRCh38#38005094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29151406-A-C

38005095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29151405-C-T

38005555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150923-C-G

38005555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150923-C-T

38005599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150885-T-C

38005618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150869-C-T

38005623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150864-A-G

38005633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150854-C-G

38005708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29150781-G-A

38006277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29146732-T-C

38007043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29146044-C-T

38007044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29146043-G-A

38007044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29146043-G-T

38012483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29144495-G-A

38012490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29144488-T-C

38013012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29144104-A-G

http://identifiers.org/hco/19/GRCh38#38013415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29143652-A-C

38013473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29143595-A-G

http://identifiers.org/hco/19/GRCh38#38013475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29143593-A-C

38018632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29142388-G-C

38018633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29142387-G-A

38018672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29142368-G-C

38018736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29142297-A-T

38019462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29141425-C-T

38019584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29141317-C-G

38019605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29141308-A-G

38019643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29141258-T-A

http://identifiers.org/hco/19/GRCh38#38019741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29141156-C-A

http://identifiers.org/hco/19/GRCh38#38020189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29141055-A-C

38020414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140859-G-T

38020446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140827-C-T

38020731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140552-C-T

38020787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29140494-A-G

38023127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29138430-C-G

38023313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29138261-C-T

38023361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29138218-A-G

38023619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137962-A-T

http://identifiers.org/hco/19/GRCh38#38023676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29137920-A-C

http://identifiers.org/hco/19/GRCh38#38024233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29137466-A-C

http://identifiers.org/hco/19/GRCh38#38024375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29137323-C-A

38024392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137306-G-A

38024445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137259-T-A

38024568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29137164-T-G

38024854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29136946-T-A

38025219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29136639-G-A

38025568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29136308-C-T

38025724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29136142-A-G

38025967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29135901-G-A

38026003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29135865-A-G

38026086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29135775-G-A

http://identifiers.org/hco/19/GRCh38#38026106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29135757-C-A

38026118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29135745-G-A

38026205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29135638-T-C

38028934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134385-T-G

38028962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134366-G-A

38028962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134366-G-T

38028981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134347-T-C

38029036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134306-C-T

38029054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134283-C-T

http://identifiers.org/hco/19/GRCh38#38029276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29134046-C-A

38029289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29134033-G-T

http://identifiers.org/hco/19/GRCh38#38029492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29133839-A-C

38029492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29133839-A-G

38035422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131253-C-G

38035509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131180-G-C

38035540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29131151-C-T

38035853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130885-G-A

38036001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130763-C-T

38036322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130438-G-C

38036669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130092-T-C

38036671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130090-A-G

38036671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29130090-A-T

38036766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29129992-A-G

38046172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125781-C-T

38046342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125595-G-A

http://identifiers.org/hco/19/GRCh38#38046361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29125576-C-A

38046382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125557-T-G

38046522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125495-G-A

38046522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125495-G-T

38046585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125447-A-G

38047001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125121-C-T

38047039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29125088-G-A

http://identifiers.org/hco/19/GRCh38#38047773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29121292-C-A

38047850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29121217-T-C

http://identifiers.org/hco/19/GRCh38#38047969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29121099-A-C

38047995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29121071-C-T

38048260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120703-C-T

38048412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120568-C-T

38048637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120327-C-T

http://identifiers.org/hco/19/GRCh38#38048712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29120259-A-C

38048767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120209-C-G

38049261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120100-C-G

38049261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29120100-C-T

38049345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29119937-T-C

38049358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29119889-T-G

http://identifiers.org/hco/19/GRCh38#38055793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29116804-C-A

38058247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29115059-C-T

38061044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29113064-T-C

38062070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29112305-G-A

http://identifiers.org/hco/19/GRCh38#38062449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29111979-C-A

38062934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111737-G-T

38062952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111719-G-C

38062957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111714-G-A

http://identifiers.org/hco/19/GRCh38#38063355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29111368-C-A

38063355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111368-C-G

38063355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111368-C-T

38063513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29111214-T-C

38064240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29110694-A-G

http://identifiers.org/hco/19/GRCh38#38064335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29110622-A-C

38064357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29110607-G-A

38064357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29110607-G-T

38067245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109637-C-G

38067895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109410-A-G

38067990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109309-G-A

38067990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29109309-G-T

38071652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106462-G-A

38071700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106412-T-C

38071790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106325-G-A

38072024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106159-G-A

38072032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106151-G-A

38072067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29106120-C-T

38072229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105999-G-A

38072440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105796-T-C

38072631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105651-G-A

38072660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105623-G-A

38072660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105623-G-C

38072794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105512-C-T

38072825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105481-C-G

38072869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105443-T-C

38072870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105442-T-A

38073011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105284-G-A

38073011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29105284-G-C

38081146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100683-T-C

38081191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100636-G-T

38081238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29100590-C-T

38081289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29100539-T-C

38081353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29100478-A-G

38081466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100365-T-A

http://identifiers.org/hco/19/GRCh38#38081468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29100363-C-A

38081479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100352-T-A

38081505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100326-G-A

38081505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100326-G-T

http://identifiers.org/hco/19/GRCh38#38081552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29100279-A-C

38081552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100279-A-G

38081552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 5 prime UTR variant
orthologous variants: 29100279-A-T

38081699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100132-G-C

38081729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100102-C-T

38081738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100093-C-G

38081738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100093-C-T

38081812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100037-G-A

38081812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29100037-G-T

http://identifiers.org/hco/19/GRCh38#38082061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29099788-C-A

38082061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099788-C-G

38082178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099671-A-G

38082190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099659-G-A

38082190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099659-G-C

38082244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099605-A-G

http://identifiers.org/hco/19/GRCh38#38082301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29099548-C-A

38082301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099548-C-G

38082304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099545-G-A

38082304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099545-G-T

38082305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099544-G-A

38082305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099544-G-T

38082409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099443-A-G

38082646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099206-T-C

38082646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099206-T-G

38082679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099173-G-A

38082711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: synonymous variant
orthologous variants: 29099141-C-G

http://identifiers.org/hco/19/GRCh38#38082769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29099083-A-C

38082814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099038-G-A

38082814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29099038-G-T

38082865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098987-A-G

38082865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098987-A-T

38082868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098984-G-A

38082868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098984-G-C

38082868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098984-G-T

38082886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098966-A-G

38082919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098933-C-T

http://identifiers.org/hco/19/GRCh38#38082953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29098896-C-A

38082953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098896-C-T

38083075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29098774-T-C

38083109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098740-G-A

38083109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098740-G-T

http://identifiers.org/hco/19/GRCh38#38083111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29098738-C-A

38083111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098738-C-T

38083131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098732-G-A

38083131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098732-G-T

38085057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098505-T-C

38085061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098501-G-T

38085160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098396-A-G

38085372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098195-C-T

38085405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098166-G-A

38085469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098139-G-A

38085469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29098139-G-T

38088119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29097301-C-G

38088445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096954-C-T

38088537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096865-T-G

http://identifiers.org/hco/19/GRCh38#38088597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29096810-C-A

38088597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096810-C-T

38088624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096796-G-A

38088624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096796-G-T

http://identifiers.org/hco/19/GRCh38#38088628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29096792-C-A

38088628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096792-C-T

38088639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096782-G-A

38088639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096782-G-C

38088639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29096782-G-T

38088738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096687-G-A

38088738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096687-G-T

38088795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096630-G-C

38088828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096597-A-G

38088846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096579-C-G

38088846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29096579-C-T

38088892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29096533-C-T

http://identifiers.org/hco/19/GRCh38#38088904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29096521-C-A

38088904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29096521-C-G

38088904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29096521-C-T

38088933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29096463-C-T

38090599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29094915-A-G

38090654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29094860-G-A

38090870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29094715-C-T

38090872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29094714-T-C

http://identifiers.org/hco/19/GRCh38#38090942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29094645-C-A

38093666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29093095-A-T

38093829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29092943-T-A

38093917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29092864-C-T

38094237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29092527-G-A

http://identifiers.org/hco/19/GRCh38#38095444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29091919-C-A

38095444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091919-C-G

38095444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091919-C-T

38095457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091903-T-A

38096149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091244-G-T

38096240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091156-C-T

38096631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29091039-C-T

38096859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29090830-C-G

38097000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29090696-A-G

38097014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29090682-T-C

38099581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29088395-A-G

http://identifiers.org/hco/19/GRCh38#38099943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29087593-C-A

38099943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29087593-C-T

http://identifiers.org/hco/19/GRCh38#38099962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29087574-C-A

38099962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 29087574-C-T

38099974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29087562-C-T

38100204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29087348-A-T

38100848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086912-T-G

38100873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086911-G-A

http://identifiers.org/hco/19/GRCh38#38100900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29086893-C-A

38100900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086893-C-T

http://identifiers.org/hco/19/GRCh38#38100916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29086876-C-A

38100916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086876-C-T

38100917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086875-T-C

38100943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086848-A-G

38100959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086827-C-T

38101058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29086744-C-T

38101100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29086702-A-G

38101205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29086597-G-A

38101208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29086594-G-A

38101208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 29086594-G-T

38101237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086565-G-A

38101237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29086565-G-T

http://identifiers.org/hco/19/GRCh38#38106485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29085634-C-A

38106485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085634-C-G

38106491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085628-C-G

38106491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085628-C-T

38106509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085610-A-G

38106509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085610-A-T

38106513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085606-T-C

38106513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 29085606-T-G

38107593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085108-G-A

38107593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29085108-G-C

38108480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29084466-G-A

38108538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29084416-G-T

38108561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29084390-G-A

38108676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29084309-G-T

38108846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29084163-G-A

38108865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29084144-T-C

38108882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29084128-A-T

38108986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29084035-T-A

http://identifiers.org/hco/19/GRCh38#38108987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29084034-C-A

38109015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29084010-A-G

38109246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29083789-G-C

38109246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29083789-G-T

http://identifiers.org/hco/19/GRCh38#38109261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29083774-C-A

http://identifiers.org/hco/19/GRCh38#38109439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29083587-C-A

38109493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083528-C-T

38109605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083410-A-T

38109618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083402-T-C

38109619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 29083401-G-A

38109669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083345-T-C

http://identifiers.org/hco/19/GRCh38#38109679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29083336-A-C

38109740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083270-C-G

38109747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083265-A-G

38109792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083221-G-T

http://identifiers.org/hco/19/GRCh38#38109857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29083155-A-C

38109963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29083039-C-T

38110002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29082991-G-T

http://identifiers.org/hco/19/GRCh38#38110051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29082944-C-A

38110051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29082944-C-T

http://identifiers.org/hco/19/GRCh38#38110068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29082927-C-A

38110068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29082927-C-T

http://identifiers.org/hco/19/GRCh38#38110092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29082890-C-A

38110092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082890-C-T

38110094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082888-G-A

38110094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082888-G-T

38110102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082879-T-C

38110112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082869-T-G

38110131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082866-T-G

38110136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082861-G-A

38110136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082861-G-T

38110137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082860-T-C

38110137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082860-T-G

38110184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082813-G-A

38110184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29082813-G-T

38110371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29082632-A-G

38110473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29082538-A-G

38111499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081262-T-A

38111811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29081011-A-G

38112424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080286-C-T

38112670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29080020-T-G

38112761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29079934-C-T

38113846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29079643-G-T

38119272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29077529-C-T

38119273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29077528-T-G

38119370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29077431-T-C

38119529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29077272-G-A

38119673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29077128-G-A

38119673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29077128-G-C

38119673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29077128-G-T

38119811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29076990-G-A

http://identifiers.org/hco/19/GRCh38#38119901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29076900-C-A

38119901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29076900-C-T

http://identifiers.org/hco/19/GRCh38#38119961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29076839-C-A

38119961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29076839-C-T

38120738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29075615-G-A

38130363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070785-T-C

http://identifiers.org/hco/19/GRCh38#38130377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29070771-A-C

38130387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070769-T-G

38130428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070731-G-A

38130428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070731-G-C

38130428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070731-G-T

38130464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070692-G-A

38130464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070692-G-T

38130633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29070527-C-T

38130699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29070461-A-G

38130714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29070446-A-G

38130756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29070404-G-T

38130791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29070369-C-G

38130832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070326-G-A

38130832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29070326-G-T

38139599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29067089-C-T

38140390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29066705-T-G

38140460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29066606-A-G

38140539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29066522-G-A

http://identifiers.org/hco/19/GRCh38#38141049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29066297-C-A

38141049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29066297-C-T

38141203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066206-G-A

38141232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066177-G-T

38141269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066140-C-G

38141269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066140-C-T

38141281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066128-C-T

38141296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29066113-G-A

38141333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 29066076-G-C

38141336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 29066073-C-G

38141336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 29066073-C-T

http://identifiers.org/hco/19/GRCh38#38141407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29066002-C-A

38141407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 29066002-C-T

http://identifiers.org/hco/19/GRCh38#38141488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29065917-C-A

38141488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065917-C-T

http://identifiers.org/hco/19/GRCh38#38141494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29065911-C-A

http://identifiers.org/hco/19/GRCh38#38141502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29065903-C-A

38141502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065903-C-T

38141528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065878-T-C

http://identifiers.org/hco/19/GRCh38#38141529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29065877-C-A

38141529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065877-C-G

38141529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065877-C-T

http://identifiers.org/hco/19/GRCh38#38141532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29065874-C-A

38141563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065843-T-A

38141563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29065843-T-C

38142181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29064041-A-G

38142430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063838-A-G

http://identifiers.org/hco/19/GRCh38#38142528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29063772-C-A

38142528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063772-C-T

38142773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063529-C-T

http://identifiers.org/hco/19/GRCh38#38142827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29063472-C-A

38142827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063472-C-T

http://identifiers.org/hco/19/GRCh38#38142849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29063450-C-A

38142849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063450-C-T

38142971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063311-G-A

38143037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29063250-C-T

38144292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29062590-A-G

38144302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29062580-T-C

38144677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29062229-G-T

38144752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29062149-C-G

38144766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29062138-T-C

38149966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29058449-G-A

38150267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29057981-A-G

38152298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29054103-T-C

38152317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29054084-G-A

38152317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29054084-G-T

38152437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053963-C-T

38152554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053851-G-A

http://identifiers.org/hco/19/GRCh38#38152725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29053700-C-A

38152725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053700-C-T

http://identifiers.org/hco/19/GRCh38#38152735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29053690-C-A

38152735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053690-C-T

38152759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053666-G-A

38152759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053666-G-C

http://identifiers.org/hco/19/GRCh38#38152974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29053473-C-A

http://identifiers.org/hco/19/GRCh38#38152996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29053465-C-A

38153004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053457-C-G

38153016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, undefined
orthologous variants: 29053446-G-A

38155084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053132-G-A

38155084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053132-G-C

38155084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053132-G-T

38155187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29053031-A-G

38155267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052898-C-T

38155268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052897-G-A

38155319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052831-T-A

38155356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052794-G-A

38156100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052461-A-G

38156356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052210-T-A

38156507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052072-T-C

38156525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052052-G-A

38156552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29052025-C-T

38162130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050371-T-C

38162169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050339-A-G

38162227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050260-C-G

38162227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050260-C-T

38162408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050036-C-G

http://identifiers.org/hco/19/GRCh38#38162413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29050031-C-A

38162414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050030-T-A

38162414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29050030-T-G

38162464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049912-G-A

38162464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049912-G-C

38162464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049912-G-T

http://identifiers.org/hco/19/GRCh38#38162473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29049903-C-A

38162473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049903-C-G

38162473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049903-C-T

38162599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049826-A-T

38162739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049716-G-T

38162800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049658-C-T

38162896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29049550-G-T

38163124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29049406-G-A

38163577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048890-G-A

38163758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048730-G-C

38163879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048592-T-C

38164013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048475-G-A

38164032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048453-G-A

38164046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048439-G-A

38164050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048435-C-G

38164050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048435-C-T

38164057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048428-C-T

38164389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048186-G-A

38164389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048186-G-C

38164389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29048186-G-T

38164479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 29048122-G-A

38164749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29047852-G-A

38164749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29047852-G-T

38164799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29047802-C-G

38164799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29047802-C-T

38164996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29047658-G-A

38164996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29047658-G-C

38165700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29047066-G-A

38168716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29045227-T-C

38168934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29045012-C-T

38169048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29044907-T-C

38169056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29044899-T-G

38172480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29042162-G-A

38172570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29042113-G-C

38172573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29042110-G-A

38172586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29042104-A-G

38173241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041676-C-T

38173482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041433-G-A

38173482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041433-G-T

http://identifiers.org/hco/19/GRCh38#38173491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29041424-C-A

http://identifiers.org/hco/19/GRCh38#38173609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#29041312-C-A

38173710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041212-T-C

38173721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29041205-G-A

38173721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29041205-G-T

http://identifiers.org/hco/19/GRCh38#38173730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29041196-C-A

38173730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041196-C-T

38173751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041175-A-G

38173826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041114-G-T

38173892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29041049-G-A

38182533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29038586-G-A

38182697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29038422-G-A

http://identifiers.org/hco/19/GRCh38#38182759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29038367-A-C

http://identifiers.org/hco/19/GRCh38#38182816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29038324-C-A

38182816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29038324-C-T

http://identifiers.org/hco/19/GRCh38#38182903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29038266-C-A

38182903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29038266-C-G

38182934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29038233-T-G

38184669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037355-G-T

http://identifiers.org/hco/19/GRCh38#38184703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29037321-A-C

38184703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037321-A-G

38184705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037319-G-C

http://identifiers.org/hco/19/GRCh38#38184856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29037154-C-A

38184862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037148-G-A

38184911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037093-T-C

38185013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29037025-T-C

38185073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036966-G-T

38185213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036842-G-T

http://identifiers.org/hco/19/GRCh38#38185237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036817-C-A

http://identifiers.org/hco/19/GRCh38#38185258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036796-C-A

38185258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036796-C-T

http://identifiers.org/hco/19/GRCh38#38185378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036680-C-A

38185378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036680-C-T

http://identifiers.org/hco/19/GRCh38#38185409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036645-C-A

38185409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036645-C-T

http://identifiers.org/hco/19/GRCh38#38185411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036643-C-A

38185411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036643-C-T

http://identifiers.org/hco/19/GRCh38#38185412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036642-C-A

38185412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036642-C-G

38185603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036479-G-A

38185603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036479-G-T

38185618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036465-A-T

http://identifiers.org/hco/19/GRCh38#38185738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036338-C-A

38185738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036338-C-T

http://identifiers.org/hco/19/GRCh38#38185767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29036325-A-C

38185767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036325-A-G

38185787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036306-T-C

38185846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29036247-G-T

38190486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29034155-C-T

38190584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29034061-C-T

38190812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29033856-G-C

38192088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031859-T-C

38192095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031852-G-A

http://identifiers.org/hco/19/GRCh38#38192137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29031821-C-A

38192137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29031821-C-G

38192137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 29031821-C-T

38192305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29031653-A-T

http://identifiers.org/hco/19/GRCh38#38192360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29031631-C-A

38192360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031631-C-T

38192422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031592-T-C

http://identifiers.org/hco/19/GRCh38#38192423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29031591-C-A

38192423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031591-C-T

38192456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031558-T-A

38192458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031556-G-A

38192458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031556-G-T

38192540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031496-G-A

38192540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031496-G-T

http://identifiers.org/hco/19/GRCh38#38192664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29031404-C-A

38192664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031404-C-G

38192664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031404-C-T

38193035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031284-C-T

38193118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031226-G-C

38193498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29031002-G-T

http://identifiers.org/hco/19/GRCh38#38193531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030973-C-A

38193579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030925-A-G

38193588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030916-A-G

38193588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030916-A-T

http://identifiers.org/hco/19/GRCh38#38193643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030861-C-A

38193643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030861-C-G

38193645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030859-A-G

38193657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29030847-T-C

http://identifiers.org/hco/19/GRCh38#38193758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030743-C-A

38193758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: synonymous variant
orthologous variants: 29030743-C-T

38193789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030712-G-A

38193789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030712-G-C

38193789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030712-G-T

38193799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030702-G-A

38193799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030702-G-T

38193816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030690-A-G

http://identifiers.org/hco/19/GRCh38#38193820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030686-C-A

38193832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030674-G-A

38193832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030674-G-T

http://identifiers.org/hco/19/GRCh38#38193901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030618-A-C

38193901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030618-A-G

38193905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030614-A-G

38193919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030601-C-T

http://identifiers.org/hco/19/GRCh38#38193925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29030595-C-A

38193925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29030595-C-T

38198122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028757-C-T

http://identifiers.org/hco/19/GRCh38#38198140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29028739-C-A

38198140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028739-C-G

38198493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29028447-G-A

38198493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29028447-G-C

38198493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: stop gained
orthologous variants: 29028447-G-T

38198503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense variant
orthologous variants: 29028437-G-T

38198551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028389-G-A

38198551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028389-G-T

38198552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028388-T-A

38198552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028388-T-C

http://identifiers.org/hco/19/GRCh38#38198623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29028319-C-A

38198623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29028319-C-T

http://identifiers.org/hco/19/GRCh38#38198624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29028318-C-A

38201822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29025354-A-G

38201831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29025348-G-A

http://identifiers.org/hco/19/GRCh38#38201832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29025347-A-C

38201832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29025347-A-G

http://identifiers.org/hco/19/GRCh38#38202027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29025157-A-C

38202027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29025157-A-G

38202055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29025130-G-A

http://identifiers.org/hco/19/GRCh38#38202091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29025090-C-A

38202776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024922-G-A

38202782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024916-G-C

38202801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024888-G-T

38202815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024874-G-A

38203336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024416-A-G

38203379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024373-G-A

38203381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024371-C-T

38203502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024268-A-T

http://identifiers.org/hco/19/GRCh38#38203544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29024227-A-C

38203566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024174-G-A

38203566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024174-G-C

38203566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024174-G-T

http://identifiers.org/hco/19/GRCh38#38203576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29024164-A-C

38203576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024164-A-G

38203576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024164-A-T

38203669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024122-G-A

38203669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron variant
orthologous variants: 29024122-G-T

38203795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29024006-C-G

38203795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29024006-C-T

http://identifiers.org/hco/19/GRCh38#38203935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023861-A-C

38203935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023861-A-G

38203935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023861-A-T

http://identifiers.org/hco/19/GRCh38#38203943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023853-C-A

http://identifiers.org/hco/19/GRCh38#38203989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023823-C-A

38203989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023823-C-T

38203999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023813-T-C

http://identifiers.org/hco/19/GRCh38#38204004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023808-C-A

38204050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023752-G-A

http://identifiers.org/hco/19/GRCh38#38204106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023695-C-A

38204106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 29023695-C-T

38204198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29023603-A-G

38204198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29023603-A-T

38204213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29023588-G-T

http://identifiers.org/hco/19/GRCh38#38204234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29023566-C-A

38204234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29023566-C-T

38205648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29022181-G-A

38205806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29022065-T-C

38205887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021900-C-T

38205905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021877-G-A

38205911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021871-A-G

38205944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021840-A-G

38206004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021783-G-A

38206004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29021783-G-T

http://identifiers.org/hco/19/GRCh38#38206077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29021729-C-A

38206124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 29021683-T-A

38206255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29021547-G-A

38206255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29021547-G-T

http://identifiers.org/hco/19/GRCh38#38206256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29021546-C-A

38206340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29021497-G-A

38206340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29021497-G-T

38206356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29021479-T-C

38206392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021451-G-T

38206407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021440-T-A

38206407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021440-T-C

38206448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021424-T-C

38206448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021424-T-G

http://identifiers.org/hco/19/GRCh38#38206465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29021409-C-A

38206465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021409-C-T

38206467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021407-G-A

38206467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021407-G-T

38206874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021148-G-A

38206874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021148-G-T

38206895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29021127-A-G

http://identifiers.org/hco/19/GRCh38#38206945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29021084-C-A

38207133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020950-G-A

38207133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020950-G-T

38207151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020939-G-T

38207258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020847-G-A

38207258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020847-G-T

http://identifiers.org/hco/19/GRCh38#38207265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29020840-A-C

38207265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020840-A-G

38207570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020564-A-G

38207581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020552-G-T

38207615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020545-A-G

38207665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020497-A-G

38207723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020447-C-T

38207778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020408-G-A

38207778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020408-G-T

38207795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020391-T-C

http://identifiers.org/hco/19/GRCh38#38207843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29020347-C-A

38207843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020347-C-T

38207956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020201-C-T

38208005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020152-C-T

38208018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29020139-C-T

38208337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29019830-G-A

38208337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29019830-G-C

38208337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23801
most severe consequence: 3 prime UTR variant
orthologous variants: 29019830-G-T