http://identifiers.org/hco/17/GRCh38#13757027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64217970-C-A

13757027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64217970-C-T

http://identifiers.org/hco/17/GRCh38#13757197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64217765-C-A

http://identifiers.org/hco/17/GRCh38#13757238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64217728-A-C

13757290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64217678-T-C

13758640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64216122-T-C

13758657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64216105-G-A

13758876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215865-G-T

13758880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215861-A-G

13758880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215861-A-T

13758992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215701-A-T

13758998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215695-A-G

13758998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215695-A-T

13759054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215647-A-G

13759126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215574-G-T

13759179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215540-T-G

13759563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215211-G-A

13759563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215211-G-C

13759603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64215171-T-C

http://identifiers.org/hco/17/GRCh38#13759632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64215144-A-C

13760067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64214368-T-A

13760067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64214368-T-C

http://identifiers.org/hco/17/GRCh38#13760133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64214309-C-A

13760133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64214309-C-T

13760407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213629-C-T

13760438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213598-G-A

13760455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213581-T-C

13760816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64207763-G-C

13760817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64207762-C-T

13761021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213262-G-A

13761152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213135-G-T

13761186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64213102-C-T

13761761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212526-G-T

13761872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212416-C-G

13761884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212404-G-A

13761904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212383-G-T

13761913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212374-A-T

13762069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64212225-A-T

13762334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211962-A-T

13762617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211699-T-C

13762994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211590-C-T

13763159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211489-C-T

13763177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211471-G-A

13763451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211197-C-G

13763451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211197-C-T

13763635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64211022-G-A

13763669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210990-A-G

13764254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210735-G-A

13764368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210628-T-A

13764368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210628-T-C

13764396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210605-G-A

13764402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210592-C-T

13764548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210453-A-G

13764549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210452-G-A

http://identifiers.org/hco/17/GRCh38#13764913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64210134-A-C

http://identifiers.org/hco/17/GRCh38#13764917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64210130-A-C

13764917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64210130-A-G

13765958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64209143-A-G

13766322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208751-G-T

http://identifiers.org/hco/17/GRCh38#13766408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64208665-A-C

13766514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208556-T-G

13766866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208206-G-A

13766948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208125-A-T

13766981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208092-G-A

13766981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64208092-G-T

13767347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64207763-G-A

13767347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64207763-G-T

13767651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64207442-T-G

13771651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205523-T-C

13771731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205461-C-G

http://identifiers.org/hco/17/GRCh38#13771820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64205367-A-C

13771863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205328-A-G

13771899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205296-G-A

13771899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205296-G-T

13771974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64205216-A-G

13772200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204856-A-G

13772237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204799-A-G

13772243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204793-A-G

13772322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204718-C-T

13772346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204703-G-A

13772360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204689-A-G

13772401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204656-T-C

13772433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204613-G-T

13772631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204428-A-G

13772651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204412-G-A

13772712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204376-G-A

http://identifiers.org/hco/17/GRCh38#13772768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64204319-C-A

13772768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204319-C-T

13772911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204218-G-A

http://identifiers.org/hco/17/GRCh38#13773036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64204161-C-A

13773104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204117-G-A

13773135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204086-G-C

13773172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64204049-T-C

13774633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64203509-C-G

13774633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64203509-C-T

13774756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64203158-A-G

13774774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64203143-C-T

http://identifiers.org/hco/17/GRCh38#13774838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64203071-C-A

13775007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64202971-T-C

13775097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64202908-C-T

13775186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64202803-T-A

13775346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64202626-G-A

13775416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64202555-G-C

13775454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201657-G-A

13775463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201648-T-C

13775657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201452-G-C

13775803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201310-T-C

13775940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201204-T-C

13775990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201155-G-A

13775990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64201155-G-T

13776370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64200796-C-G

13776370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64200796-C-T

13776477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200691-A-G

http://identifiers.org/hco/17/GRCh38#13776520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64200657-C-A

13776520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200657-C-T

13776560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 64200616-G-T

13776607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200592-A-T

http://identifiers.org/hco/17/GRCh38#13776695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64200523-C-A

13777061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200177-G-A

13777141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200094-G-A

13777141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64200094-G-T

13777737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 64199256-C-T

13777767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64199226-G-C

13777786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64199207-G-A

13777906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64199083-C-G

13777906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64199083-C-T

http://identifiers.org/hco/17/GRCh38#13784038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64197185-A-C

13784038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64197185-A-T

http://identifiers.org/hco/17/GRCh38#13784074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64197149-C-A

13784129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64197095-T-C

13784161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64197065-T-A

13784329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64196893-A-T

13784847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64189251-C-G

13784952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64189139-T-A

13785011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64189080-T-C

13785117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188971-T-G

13785160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188930-C-T

13785247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188840-C-T

http://identifiers.org/hco/17/GRCh38#13785364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64188749-A-C

13785364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188749-A-G

13785364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188749-A-T

13785374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188739-G-T

13785405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188708-G-A

13785466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188654-T-C

13785630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188393-C-T

13785774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64188002-G-C

13785779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64187997-C-T

13786187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64187609-C-T

13786233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64187563-C-G

http://identifiers.org/hco/17/GRCh38#13790887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64186587-C-A

http://identifiers.org/hco/17/GRCh38#13790959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64186515-C-A

13790959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64186515-C-T

13791015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64186460-T-A

13791024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64186451-A-G

13791067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64186406-A-G

13795635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64183370-A-G

13795642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64183363-C-G

13795649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64183356-C-T

13795850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64183161-T-C

13796067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64182943-G-A

13796256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64182754-T-C

13797791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64182214-G-C

13797791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64182214-G-T

13801825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64181260-T-G

13801958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64181123-A-G

http://identifiers.org/hco/17/GRCh38#13802013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64181071-A-C

13802058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64181028-T-A

13802058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64181028-T-C

http://identifiers.org/hco/17/GRCh38#13802091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64180994-A-C

13802091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64180994-A-G

13802923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64180636-T-C

13802952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64180608-C-T

13803359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64180206-T-A

13803544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64180021-C-T

13803758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179869-G-A

13803847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179786-C-G

13807247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179430-G-A

13807288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179391-G-A

13807417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179294-C-G

13807417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179294-C-T

13807471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179238-A-T

13807660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179076-T-C

13807702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64179015-T-C

13807853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178885-C-T

13808018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178795-C-G

13808032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178784-G-A

13808079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178747-T-C

13808137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178693-G-A

http://identifiers.org/hco/17/GRCh38#13808264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64178572-C-A

13808264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64178572-C-T

13810119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64177818-C-T

13810577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64177336-A-G

13810639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64177279-T-C

13817091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175788-G-A

13817238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175653-T-C

13817436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175479-G-A

13817451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175464-T-C

13817508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175401-T-G

13817516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175393-A-T

13817541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175374-T-G

13817733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175188-T-C

13817771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175150-A-T

13817889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175026-T-C

13817907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64175009-G-A

13817951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64174965-T-C

13817966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64174949-T-A

13818003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64174915-A-G

13819923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64173068-T-C

13819932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64173059-C-T

13820413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172596-A-G

13820490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172492-T-A

13820533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172452-G-A

13820641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172356-G-A

http://identifiers.org/hco/17/GRCh38#13820758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64172237-C-A

13820758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172237-C-T

13820762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172233-A-G

13820848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172175-T-C

http://identifiers.org/hco/17/GRCh38#13820937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64172078-A-C

13821004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64172011-C-T

13821687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64170155-A-G

http://identifiers.org/hco/17/GRCh38#13821764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64170078-C-A

13822803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169429-G-A

13822803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169429-G-C

13822971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169237-C-T

13823037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169170-T-C

13823058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169149-G-C

13823060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169147-T-C

13823173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64169040-T-C

13823806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168882-T-C

13823818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168869-G-A

13823936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168757-T-A

13824021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168673-A-G

13824075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168642-C-T

13824211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168527-T-C

13824388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168356-C-T

13824586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168163-G-A

13824586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168163-G-C

13824588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64168161-A-G

13824920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167838-T-C

13825059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167717-G-A

13825059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167717-G-T

http://identifiers.org/hco/17/GRCh38#13825115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64167660-A-C

http://identifiers.org/hco/17/GRCh38#13825117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64167658-C-A

13825204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167575-T-C

13825243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167535-A-G

http://identifiers.org/hco/17/GRCh38#13825282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64167497-C-A

http://identifiers.org/hco/17/GRCh38#13825486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64167310-C-A

13825486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167310-C-T

http://identifiers.org/hco/17/GRCh38#13825492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64167304-A-C

13825854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64167016-G-T

13825966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166905-T-C

13825987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166884-C-T

13826168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166716-A-T

13826180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166704-T-G

13826345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166547-A-G

13826684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64166234-G-A

13826996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64165979-C-T

13827221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64165896-G-A

13828334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64165430-G-A

13828451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64165309-G-T

13828738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64165055-C-T

13829135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64164657-C-T

13829964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64164232-C-T

13830123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64164089-G-A

http://identifiers.org/hco/17/GRCh38#13830326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64163911-A-C

13830421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163850-T-C

13830581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163721-T-C

13830581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163721-T-G

13830956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163691-C-T

13831074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163589-G-A

13831094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163578-A-G

13831128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64163543-T-A

13839114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64160590-T-C

13839619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64159684-G-C

13839799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64159508-G-T

13840119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64159189-A-G

13840333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158989-C-G

13840333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158989-C-T

13840551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158787-T-A

13840557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158781-T-C

13841021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158340-T-C

13841075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64158310-G-A

13842566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64157808-A-G

13843118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64157312-C-T

13843371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64157017-C-T

http://identifiers.org/hco/17/GRCh38#13843589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64156815-A-C

13843605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64156799-T-C

13843728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64156703-C-G

13843916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64156517-G-A

13844001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64156440-A-G

13844267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64156206-G-A

13844449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64155144-T-C

13844795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154801-T-C

13844827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154765-G-A

http://identifiers.org/hco/17/GRCh38#13844948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64154661-C-A

13844960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154649-C-G

13844979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154630-C-T

13844992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154617-T-C

13844992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154617-T-G

13845383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154284-G-A

13845397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154273-C-G

13845556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154116-C-T

13845591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154088-G-A

http://identifiers.org/hco/17/GRCh38#13845621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64154055-C-A

13845623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64154053-A-G

http://identifiers.org/hco/17/GRCh38#13845820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64153485-C-A

13845820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64153485-C-T

13845892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64153416-C-T

13846394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64152934-C-T

13846495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64152836-C-G

13846495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64152836-C-T

http://identifiers.org/hco/17/GRCh38#13846704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64152651-A-C

13846747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64152578-A-G

13846796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64152534-T-C

13847226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151979-A-T

13847311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151855-T-C

13847591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151559-A-G

13847780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151381-A-G

http://identifiers.org/hco/17/GRCh38#13847848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64151311-A-C

13847853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151306-G-A

13847857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151301-A-G

13847860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151298-T-C

13847879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151264-T-C

13847888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151251-T-C

13848054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64151065-T-G

13848132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150998-G-A

http://identifiers.org/hco/17/GRCh38#13848172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64150958-A-C

13848172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150958-A-T

13848314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150832-A-G

13848503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150738-G-T

13848536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150696-T-A

13848812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150421-T-G

13848987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150279-T-C

13849112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150157-A-G

13849176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150102-C-T

13849242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150041-C-G

13849243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64150040-A-G

13849339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149943-T-C

13849431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149511-T-A

http://identifiers.org/hco/17/GRCh38#13849557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64149367-C-A

13849557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149367-C-T

13849659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149281-G-A

13849700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149250-A-G

http://identifiers.org/hco/17/GRCh38#13849804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64149169-C-A

13849804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149169-C-T

13849841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64149136-A-G

13850036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64148986-C-T

13850514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64148544-A-T

13850717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64148382-G-C

13862605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145441-T-C

13862721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145303-C-G

13862721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145303-C-T

13862728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145296-G-A

13862831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145212-G-C

13862837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145206-G-A

13862837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145206-G-T

13862986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145102-C-T

13863038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145046-T-C

13863050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145034-A-T

http://identifiers.org/hco/17/GRCh38#13863070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64145015-C-A

13863070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64145015-C-T

13863413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144760-T-A

13863463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144692-T-A

13863467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144688-T-C

13863522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144631-G-A

13863838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144259-A-G

13863933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144174-T-C

13863935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144172-C-G

13863990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64144110-G-A

13864188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143911-T-C

http://identifiers.org/hco/17/GRCh38#13864264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64143857-C-A

13864278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143841-A-G

13864716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143420-G-A

13864724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143413-A-G

13864767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143370-C-T

13864896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143262-G-A

13865014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64143148-T-G

13865092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64143097-T-C

http://identifiers.org/hco/17/GRCh38#13865146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64143044-C-A

13865160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64143030-T-A

13865211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64142981-A-G

http://identifiers.org/hco/17/GRCh38#13865219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64142973-C-A

http://identifiers.org/hco/17/GRCh38#13865234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64142958-C-A

http://identifiers.org/hco/17/GRCh38#13865246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64142946-C-A

13865326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64142875-G-T

13866241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140710-T-C

13866289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140663-A-G

http://identifiers.org/hco/17/GRCh38#13866557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64140423-C-A

13866557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140423-C-T

13866661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140261-A-G

13866673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140250-T-A

13866673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140250-T-G

13866745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140192-T-C

13866867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140072-C-G

13866921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64140021-A-G

13867084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64139865-C-T

13867721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64137180-T-C

13868424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136949-A-G

13868444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136929-T-C

13868495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136880-A-G

13868555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136821-G-C

13868695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136680-G-A

13868718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136657-A-G

13869108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136451-G-T

13869252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64136318-A-G

13869641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64135929-C-T

13869969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64135591-A-G

13876405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64132348-A-G

http://identifiers.org/hco/17/GRCh38#13876424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64132329-C-A

http://identifiers.org/hco/17/GRCh38#13876490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64132274-C-A

13876675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64132115-G-A

13876877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64131910-T-G

13877235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64131463-C-T

13877373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64131073-G-A

13877394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64131045-G-A

13877735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64129097-G-A

13877989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64128882-C-T

13878066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64128811-G-T

13878091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64128786-T-C

13878324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

13878399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

13878555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

13879493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127581-C-G

13879493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127581-C-T

http://identifiers.org/hco/17/GRCh38#13879505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64127572-C-A

13879531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127546-T-G

13879575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127500-T-A

13879575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127500-T-C

13879598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127477-T-C

13879709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127384-A-G

13879808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127301-C-T

13880043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64127069-C-T

http://identifiers.org/hco/17/GRCh38#13880139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64126965-A-C

http://identifiers.org/hco/17/GRCh38#13880267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64126864-C-A

http://identifiers.org/hco/17/GRCh38#13880296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64126835-C-A

13880326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64126807-A-G

http://identifiers.org/hco/17/GRCh38#13883240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64124655-C-A

13883267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124628-C-T

13883268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124627-A-G

13883342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124561-G-A

http://identifiers.org/hco/17/GRCh38#13883350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64124553-C-A

http://identifiers.org/hco/17/GRCh38#13883509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64124408-A-C

13883546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124372-G-C

13883580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124332-G-A

13883629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124292-G-T

13883821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64124131-A-G

13884494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64123820-C-T

13884600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64123744-A-G

13885310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64123383-C-T

13885829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122945-T-C

13885880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122900-G-T

13886530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122327-G-A

13886577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122279-C-T

13886714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64122143-G-C

13886894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121995-T-C

13886925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121977-A-G

13886966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121935-C-T

13887063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121847-C-T

13887139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121784-T-A

13887170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121755-C-T

13887186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121740-C-G

13887227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121698-C-T

http://identifiers.org/hco/17/GRCh38#13887243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64121676-C-A

13887351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121524-G-A

13887469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121441-A-T

13887519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121398-A-G

13887568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121350-A-G

13887601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121328-T-C

13887725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121099-T-G

13887771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64121055-A-G

13896357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114424-T-A

13896454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64114066-C-T

13896896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113639-A-G

13896899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113636-G-A

http://identifiers.org/hco/17/GRCh38#13896972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64113563-C-A

13897424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64113450-T-C

http://identifiers.org/hco/17/GRCh38#13897893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64113134-C-A

13898184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112898-C-T

13898281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112813-T-C

13898359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112765-G-A

13898727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64112704-T-G

13898754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112677-A-G

13898760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112671-G-A

13898760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112671-G-T

13898780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112660-G-A

13898799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112641-A-G

13898833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112607-G-A

13898924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112505-C-T

13898925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112504-T-C

13899020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112420-T-G

13899043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112395-G-C

13899055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112383-A-G

13899055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112383-A-T

13899079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112343-A-G

13899267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112104-C-T

13899275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112096-G-A

13899355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64112014-C-T

13903570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64111014-T-C

13903832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110768-T-C

13904066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110546-G-A

13904066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110546-G-T

13904208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110194-C-T

http://identifiers.org/hco/17/GRCh38#13904211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64110191-A-C

13904211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110191-A-G

13904211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110191-A-T

http://identifiers.org/hco/17/GRCh38#13904277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64110143-C-A

13904347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64110072-T-G

13905006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108311-T-A

http://identifiers.org/hco/17/GRCh38#13905180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64108155-C-A

13905180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108155-C-G

13905215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64108122-T-C

13905876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107819-G-A

13906221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107458-G-A

13906230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107449-A-G

13906253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107426-C-T

13906262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107417-G-T

13906386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107291-G-C

13906435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64107242-A-G

13916252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102524-G-A

13916344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102452-G-A

13916507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102376-A-T

13916582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102310-T-C

13916648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102244-T-C

13917558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102138-T-C

13917558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64102138-T-G

13917879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101819-T-C

13918016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101691-T-A

13918065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101665-G-A

13918125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101608-C-T

13918141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101594-C-T

13918145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64101590-T-C

13932739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64098338-T-G

13932971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64098089-A-G

13932989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 64098072-A-G

13933008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64098053-G-T

13933360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64097856-G-C

13933528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64097750-T-C

13934717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096442-T-C

13934731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096429-A-T

13935203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096014-T-G

13935222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64096004-A-G

13935277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095942-T-C

http://identifiers.org/hco/17/GRCh38#13935401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64095822-C-A

13935401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095822-C-T

13935452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095790-G-C

13935526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095711-T-A

13935526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64095711-T-G

13940384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64092337-C-T

13940555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64092174-G-C

13940576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64092153-G-A

13940643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64092085-C-T

13940850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091904-A-G

http://identifiers.org/hco/17/GRCh38#13940982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64091775-C-A

13940990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091767-C-T

13941064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64091695-T-A

http://identifiers.org/hco/17/GRCh38#13941951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64089879-C-A

13941953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089877-A-G

13942148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089697-G-C

13942284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089550-T-C

13942630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089207-T-C

http://identifiers.org/hco/17/GRCh38#13942689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64089149-A-C

13942837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64089020-A-G

13943076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088819-G-A

13943305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64088233-G-C

http://identifiers.org/hco/17/GRCh38#13943320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64088222-A-C

13943744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087927-C-T

13944002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087690-G-A

13944103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087589-T-C

13944357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087364-G-A

13944511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64087218-A-G

13944990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086883-A-G

13945109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086786-G-A

13945115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086780-C-T

13945313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086535-C-T

13945395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086472-T-A

13945478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086411-G-A

13945564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086329-C-G

13945606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086298-C-T

13945685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086230-G-C

13945728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086188-T-G

13945769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64086150-G-T

13946188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085822-G-A

13946512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085193-A-G

13946574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085132-A-G

13946645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085063-T-G

13946668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64085040-G-A

13947031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084752-G-T

13947077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084703-G-A

13947081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084699-T-C

13947597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084322-T-A

13947722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64084211-C-T

13949225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64083342-C-T

13949337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082857-A-G

13949337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082857-A-T

13949710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082478-A-T

13949760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082443-G-T

13950091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64082115-C-T

13950275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081939-T-C

13950741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64081489-G-A

13951957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64080090-T-G

13952203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079269-G-A

13952203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64079269-G-T

13952251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64079210-T-C

13952327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64079134-C-T

13952471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64078991-C-T

http://identifiers.org/hco/17/GRCh38#13952530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64078932-A-C

13952552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64078910-A-T

13952594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078868-A-G

13952594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078868-A-T

http://identifiers.org/hco/17/GRCh38#13952832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64078673-C-A

13952832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078673-C-T

13952872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078613-A-G

13952953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078535-G-A

13953067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078435-A-G

13953104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078399-G-A

13953129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078374-C-T

13953179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078336-T-C

13953181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64078334-T-C

http://identifiers.org/hco/17/GRCh38#13953362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64078220-C-A

13953680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64077920-C-T

http://identifiers.org/hco/17/GRCh38#13953825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64077790-C-A

13953825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64077790-C-G

13957099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64077055-G-A

13957165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64077001-T-C

13957447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075980-A-T

13957468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075950-T-G

13957495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075926-C-G

13957645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075769-T-C

http://identifiers.org/hco/17/GRCh38#13957783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64075638-C-A

13957783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64075638-C-G

13957800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64075621-G-A

13958031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64075368-C-G

13958031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 64075368-C-T

13958311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075127-T-G

13958356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075084-G-A

13958358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075082-A-G

13958377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075063-G-A

13958418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64075027-G-C

http://identifiers.org/hco/17/GRCh38#13958520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64074950-C-A

13958520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074950-C-T

13958871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074602-T-C

13959018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074474-G-A

13959027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074462-C-T

13959110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074361-C-G

13959110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074361-C-T

13959330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074156-C-T

13959492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64074015-G-A

13959845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073704-G-T

http://identifiers.org/hco/17/GRCh38#13959902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64073642-A-C

13960080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073398-A-G

13960138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073331-C-T

13960412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64073060-A-G

13960497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072971-G-T

13960608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072859-A-G

13960608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072859-A-T

13960878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072590-C-T

13961239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64072252-G-A

13962563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071609-G-A

13962633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071541-T-C

13962776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071406-A-G

13962815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071365-A-G

13962860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071322-C-T

13962963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64071204-G-C

13963604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070462-C-T

13963707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070362-C-G

13963731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64070338-A-T

13964216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64069719-A-T

13968333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067611-G-A

13968333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067611-G-T

13968609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067314-T-G

13968678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067226-A-G

13968687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067217-G-A

13968765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64067137-A-T

13969043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64066866-T-C

13969780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64065642-C-T

13969853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64065117-G-A

13969853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64065117-G-C

13969968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64065005-T-G

13977182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64064693-G-A

13977748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64064107-G-A

13977771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64064084-A-G

13977771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64064084-A-T

13977786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64064068-T-A

13977920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063918-T-C

13977928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64063909-A-G

13981742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64059962-T-C

13982551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64059178-C-T

13982614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64059127-C-T

13982755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64059031-T-C

13982789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058998-A-T

13982969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058834-G-A

13983073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058745-G-A

http://identifiers.org/hco/17/GRCh38#13983145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64058668-C-A

13983398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058448-G-C

13983521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058331-A-T

13983575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058277-G-A

13983598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058253-G-T

13983638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058213-C-T

13983639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64058212-G-A

13984357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056667-T-C

13984381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056647-G-A

13984584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056447-C-T

13984665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056365-T-C

13984709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056333-G-A

13984749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056307-A-G

13984820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64056237-T-A

13985032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055999-A-G

13985167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055863-G-A

13985167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055863-G-C

13985167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055863-G-T

13985372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055671-T-C

13985560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64055524-A-G

http://identifiers.org/hco/17/GRCh38#13986091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64054659-C-A

13986168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64054583-G-A

13986169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64054582-A-G

13986449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64054325-T-C

13986645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64054137-C-T

http://identifiers.org/hco/17/GRCh38#13988809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64053240-A-C

13988847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64053214-T-A

http://identifiers.org/hco/17/GRCh38#13988987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64053076-C-A

13988987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64053076-C-T

13990023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64051897-G-A

13990203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64051717-G-T

13990224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64051696-A-G

13990867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64051498-C-T

13991055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64051331-A-G

13993888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64050135-A-T

13994071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64049974-A-T

13994350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64049337-A-T

13994385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64049302-C-T

13994551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64049140-G-A

13994754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048997-A-G

13994764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048987-A-G

13994809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048947-T-A

13995393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048453-T-A

13995393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048453-T-G

13995572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048272-T-A

13995706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64048147-G-A

13996316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64047525-C-T

13996587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64046519-G-T

13996594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64046512-C-T

13996998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64046124-C-G

13997927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64045754-T-C

13998142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64045544-A-G

13998778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64045247-T-C

13999268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64044771-C-T

13999269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64044770-A-G

13999399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64044585-T-C

13999643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64044298-A-T

14000185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64044058-A-T

14000251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64043998-T-C

14000284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64043967-C-G

14000284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64043967-C-T

14001721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64042376-C-T

14001770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64042339-C-T

14002057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64042099-A-G

14002117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64042042-A-G

14002133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64042025-G-A

14002393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64041897-G-A

14002739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64041438-T-A

http://identifiers.org/hco/17/GRCh38#14003101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64041159-C-A

http://identifiers.org/hco/17/GRCh38#14003124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64041138-A-C

14003222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64041032-T-A

14003265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040985-G-C

14003299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040952-T-C

14003611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040844-C-G

14003611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040844-C-T

http://identifiers.org/hco/17/GRCh38#14003760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64040726-A-C

14003928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040549-A-T

14004120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040369-A-G

14004234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040269-A-G

14004235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040268-C-T

14004236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040267-C-G

14004282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040217-G-T

http://identifiers.org/hco/17/GRCh38#14004483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64040103-C-A

14004542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64040048-A-G

14004635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64039962-G-C

14004777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64039680-G-A

14004777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64039680-G-C

14004777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64039680-G-T

http://identifiers.org/hco/17/GRCh38#14004820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64039498-A-C

14004932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64039352-A-T

14006024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64038397-G-C

http://identifiers.org/hco/17/GRCh38#14006059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64038334-C-A

14006074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64038318-T-C

14006109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64038264-A-G

14006193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64038168-G-A

14006247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64038119-G-A

14006372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64037966-T-C

http://identifiers.org/hco/17/GRCh38#14009938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64037478-C-A

14010059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64037351-A-G

14010084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64037326-A-G

14010223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64037190-T-C

14010469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64036015-C-T

14010490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035994-T-C

14010627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035868-T-A

14010627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035868-T-C

http://identifiers.org/hco/17/GRCh38#14010654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64035841-A-C

14011024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035632-A-G

14011088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035583-A-T

14011371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035309-T-A

14011406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035274-C-T

14011466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035215-A-G

14011533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035148-G-A

14011570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035120-C-T

14011682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64035012-T-A

14011717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64034946-G-A

14011744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64034920-G-A

14014824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64026826-A-G

14014989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64026655-A-T

14015105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64026552-A-G

http://identifiers.org/hco/17/GRCh38#14015689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64025996-A-C

http://identifiers.org/hco/17/GRCh38#14015811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64025873-C-A

14015987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025695-A-G

http://identifiers.org/hco/17/GRCh38#14016130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64025550-C-A

14016369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025323-C-T

14016431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025280-G-C

14016551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025143-A-T

14016586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025099-T-C

14016661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025038-T-C

14016679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025024-G-C

14016679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64025024-G-T

http://identifiers.org/hco/17/GRCh38#14017299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64024595-A-C

14017299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64024595-A-G

14017392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64024555-G-A

http://identifiers.org/hco/17/GRCh38#14017497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64024436-A-C

14017896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64024051-T-C

http://identifiers.org/hco/17/GRCh38#14017985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64023973-C-A

14018089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023876-T-G

14018123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023842-T-C

http://identifiers.org/hco/17/GRCh38#14018262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64023707-C-A

14018262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023707-C-T

http://identifiers.org/hco/17/GRCh38#14018268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#64023701-A-C

14018268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023701-A-T

14018372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023620-C-T

14018592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64023440-A-G

14019641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64021077-G-A

14019784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64020953-C-T

14019791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 64020947-G-A

14019864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64020901-G-A

14020612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64020360-T-C

14032098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63996689-T-A

14032098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63996689-T-C

14032098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63996689-T-G

14032940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63995420-G-C

http://identifiers.org/hco/17/GRCh38#14033121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63995247-A-C

14033121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63995247-A-G

14035576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63994164-T-C

14035718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63994032-G-C

14036017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63993833-A-G

14037388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63992019-G-A

14037505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63991917-T-C

14037904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63991181-A-T

14037955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63991130-T-A

14038002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63991098-G-A

14038002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63991098-G-T

14038149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63990945-C-T

14038323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63990791-G-A

14038462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63990678-A-G

14043045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63988637-T-A

14044992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63988357-C-T

14045179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63988175-T-C

http://identifiers.org/hco/17/GRCh38#14045794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63987636-C-A

14045796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63987634-T-C

14049719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63986699-T-C

14050030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63986406-A-G

14051716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63984382-C-T

14052070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63983526-G-A

14052184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63983412-A-G

14052254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63983343-C-G

14052264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63983333-C-T

http://identifiers.org/hco/17/GRCh38#14052298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63983303-C-A

14053022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63982549-G-A

14053055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63982516-T-C

14053608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63981942-G-A

14053834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63981715-C-T

14053835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63981714-G-A

14057068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63979638-A-G

14057205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63979401-A-G

14057329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63979265-C-T

http://identifiers.org/hco/17/GRCh38#14057343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63979247-C-A

14057343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63979247-C-T

http://identifiers.org/hco/17/GRCh38#14058450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63978205-A-C

14058450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63978205-A-G

14058484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63978198-T-C

14058497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63978185-G-A

14059580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63975446-G-C

14059656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63975374-G-C

14060105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63975028-A-T

14060407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63974856-T-A

14060736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63974523-G-C

14061026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63974262-T-C

14061168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63974118-T-C

14061283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63973859-G-A

14061311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63973829-C-T

http://identifiers.org/hco/17/GRCh38#14061701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63973588-C-A

14061701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63973588-C-T

14061921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63973355-G-C

http://identifiers.org/hco/17/GRCh38#14062182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63973121-C-A

14068140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63970828-A-T

http://identifiers.org/hco/17/GRCh38#14068157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#63970811-C-A

14068169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63970799-G-T

14069494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 63970314-G-A

14069494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 63970314-G-C

14069494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38873
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 63970314-G-T