http://identifiers.org/hco/2/GRCh38#14172805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14689253-A-C

14172808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14689250-A-G

14173061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688933-T-C

14173295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14688706-C-T

14176984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677847-T-A

14177265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677603-G-T

14177566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677272-T-C

14177571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677267-G-A

14177646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677181-G-T

14177728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677104-A-G

14177811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14677030-T-C

14177978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676902-G-A

14177978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676902-G-T

14177981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676899-C-T

14178445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676505-T-C

14178508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676451-T-C

14178586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676373-G-A

14178799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14676127-A-G

14178941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675876-C-T

14178943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675874-G-A

14179136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675689-C-G

14179181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675646-T-C

14179249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675577-G-A

14179347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675479-G-T

14179366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675460-A-T

14179443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675385-C-T

http://identifiers.org/hco/2/GRCh38#14179478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14675349-A-C

14179516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675311-G-C

14179669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675176-T-C

14179823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675037-G-A

14179823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14675037-G-C

http://identifiers.org/hco/2/GRCh38#14179869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14675002-A-C

14179912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14674960-T-C

14184887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14671575-G-T

14185296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14671202-G-T

14185380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14671095-C-G

14187365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669820-C-T

14187415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669774-T-A

14187536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669648-T-C

14187566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669618-A-G

14188058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669142-T-C

14188168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14669038-G-T

14189064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14668193-A-G

14189577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667707-T-C

14189922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667365-G-A

http://identifiers.org/hco/2/GRCh38#14189959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14667327-C-A

14189959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667327-C-G

14190024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667279-A-G

http://identifiers.org/hco/2/GRCh38#14190096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14667206-A-C

14190096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667206-A-G

14190096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667206-A-T

http://identifiers.org/hco/2/GRCh38#14190105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14667197-C-A

14190105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667197-C-G

14190105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14667197-C-T

http://identifiers.org/hco/2/GRCh38#14190109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14667193-C-A

14190504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666777-G-C

http://identifiers.org/hco/2/GRCh38#14190592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14666698-C-A

14190592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666698-C-T

14190678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666605-T-C

14190797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666460-G-A

14190879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666370-A-T

14190880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666369-C-T

14190911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14666328-A-T

http://identifiers.org/hco/2/GRCh38#14194491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14665049-C-A

14194634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664908-C-T

14194755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664786-C-T

14194947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664603-T-C

14195261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664324-G-T

14195368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664215-G-A

14195383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14664200-T-C

14195585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14663299-C-T

14195614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14663274-G-A

14195772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14663103-T-A

14196015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14662858-A-G

14196179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14662702-T-C

14196180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14662701-G-A

14196693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14662216-C-G

14196730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14662185-A-G

14196915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14661538-C-T

14196920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14661530-C-T

14197121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14661338-A-G

14197170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14661282-G-C

14197563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14660900-T-C

14197976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14660494-A-G

14201988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14642031-T-C

14202003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14642023-C-G

14202729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640970-T-C

14202791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640917-A-G

14202902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640808-G-A

14202902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640808-G-C

14202902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640808-G-T

http://identifiers.org/hco/2/GRCh38#14202921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14640784-A-C

14202921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640784-A-G

14202921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640784-A-T

14202931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640774-G-A

14202931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640774-G-T

http://identifiers.org/hco/2/GRCh38#14202937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14640768-A-C

14202937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640768-A-G

14202938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640767-T-A

14202938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640767-T-G

14202954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640751-G-A

14202954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640751-G-T

14203362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640362-A-T

http://identifiers.org/hco/2/GRCh38#14203402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14640329-A-C

14203616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640179-T-C

14203728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640076-G-A

14203728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640076-G-T

14203766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640040-A-G

14203803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14640002-T-C

14203863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14639948-A-G

14203885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14639927-G-A

http://identifiers.org/hco/2/GRCh38#14203901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14639911-C-A

14203951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14639859-A-G

14208960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14636994-C-T

http://identifiers.org/hco/2/GRCh38#14209025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14636927-C-A

14209325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14636456-G-A

14209325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14636456-G-T

14209608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14636182-T-C

14210137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14635738-T-A

14210137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14635738-T-G

14210149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14635726-T-G

14210177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14635698-C-G

14210774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634532-C-T

14210869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634438-A-G

14210974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634324-T-C

14210977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634321-T-C

14211064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634231-T-G

http://identifiers.org/hco/2/GRCh38#14211258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14634073-C-A

14211259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634072-T-C

14211295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14634035-T-A

14211392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14633955-C-T

14211677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14625069-G-A

http://identifiers.org/hco/2/GRCh38#14212717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14624855-A-C

14212739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624833-C-G

14212739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624833-C-T

14212804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624779-A-T

14213000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624589-C-T

http://identifiers.org/hco/2/GRCh38#14213003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14624587-C-A

14213504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624150-G-A

14213583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14624080-T-C

http://identifiers.org/hco/2/GRCh38#14215841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14619807-A-C

14215841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619807-A-G

14215895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619752-T-C

14215896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619751-A-G

14216076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619587-T-G

14216123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619547-T-G

14216149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619521-A-G

14216230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14619449-G-A

14218819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615829-A-T

14218829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615819-G-A

14218829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615819-G-T

14218831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615817-T-G

14218836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615812-G-A

14218836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615812-G-T

14218866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615782-G-A

14218872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615776-G-A

14219036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615607-T-C

14219418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14615232-G-T

14219677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614989-T-C

14219756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614919-T-C

14219801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614880-G-A

14219801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614880-G-T

14219803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614878-T-A

14219860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614810-A-T

http://identifiers.org/hco/2/GRCh38#14219982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14614701-C-A

14219982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614701-C-G

14220117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14614573-T-A

http://identifiers.org/hco/2/GRCh38#14220395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14614307-A-C

14220697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613853-T-C

14220708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613842-T-C

14220730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613819-A-T

14220871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613698-T-C

14220893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613673-G-C

14221013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613554-C-T

14221265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613292-G-C

http://identifiers.org/hco/2/GRCh38#14221289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14613270-C-A

http://identifiers.org/hco/2/GRCh38#14221294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14613265-A-C

14221335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613238-T-C

http://identifiers.org/hco/2/GRCh38#14221352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14613227-C-A

14221352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613227-C-T

14221551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14613033-C-T

14221627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612957-G-C

14221794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612790-T-C

14221795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612789-G-A

14221883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612693-T-C

14222155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612462-G-A

14222155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612462-G-C

14222303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612384-A-G

14222372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612315-C-T

14222381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612306-T-C

14222537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612153-A-T

14222599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14612089-T-A

14222791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14611904-T-A

14222791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14611904-T-C

14222962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604790-A-G

14222975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604778-T-A

14222986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604767-T-A

14223021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604741-G-C

14223083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604665-G-A

14223111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604637-T-A

14223261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604486-T-C

14223325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604425-A-G

14223445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604310-C-T

http://identifiers.org/hco/2/GRCh38#14223525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14604231-C-A

14223783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604043-C-T

14223804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14604022-T-A

14223888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14603949-T-C

14224010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14603828-G-A

14224010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14603828-G-C

14224442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14603454-G-A

14224457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14603439-T-C

http://identifiers.org/hco/2/GRCh38#14224758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14602695-C-A

http://identifiers.org/hco/2/GRCh38#14224983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14602456-C-A

14224983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602456-C-T

14225011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602422-A-T

14225290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602128-T-A

14225290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602128-T-G

http://identifiers.org/hco/2/GRCh38#14225365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14602051-C-A

14225400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602018-T-C

14225551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14602003-T-C

14226101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14601661-T-G

14226376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14601185-C-T

14226611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600933-T-G

http://identifiers.org/hco/2/GRCh38#14226766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14600797-A-C

14226878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600721-A-G

14227270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600363-T-C

14227294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600340-T-C

14227465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600235-T-G

14227479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600221-G-A

14227526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14600171-G-C

14227718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599790-C-T

14227815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599719-G-A

14227815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599719-G-C

14227924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599589-T-G

14227984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599532-C-T

14228062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599456-T-C

14228102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599417-A-G

14228128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599391-G-C

14228183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14599337-G-A

14228890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14598532-A-T

14231736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597505-G-T

14231765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597476-G-A

14231779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597462-A-G

14231842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597398-T-A

14231855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597385-G-A

14231857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597383-T-G

http://identifiers.org/hco/2/GRCh38#14231865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14597375-A-C

14231948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597285-T-C

14231949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597284-G-C

14232061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14597174-G-T

14232223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14597016-A-T

14232484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596783-G-A

14232507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596762-T-A

14232568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596695-C-T

14232697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596587-T-G

14232778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596395-T-C

http://identifiers.org/hco/2/GRCh38#14232900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14596242-C-A

14232900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14596242-C-T

http://identifiers.org/hco/2/GRCh38#14233026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14596083-A-C

14233103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14595986-G-A

14233123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14595966-G-C

14233157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14595934-G-A

14233290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14595812-G-C

14233552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14589152-G-A

http://identifiers.org/hco/2/GRCh38#14233616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14589085-C-A

14233616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14589085-C-T

14233640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14589058-C-T

http://identifiers.org/hco/2/GRCh38#14233772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14588925-C-A

http://identifiers.org/hco/2/GRCh38#14233773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14588924-A-C

http://identifiers.org/hco/2/GRCh38#14233806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14588824-C-A

14233814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14588808-T-G

14233942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14588658-C-T

14233963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14588637-G-C

14234077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14588554-C-T

14234448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14588190-T-C

14235097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587662-G-T

http://identifiers.org/hco/2/GRCh38#14235399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14587292-A-C

http://identifiers.org/hco/2/GRCh38#14235447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14587240-C-A

14235447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587240-C-T

14235492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587195-G-A

14235545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587141-G-A

14235559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587126-A-G

14235594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14587102-G-A

http://identifiers.org/hco/2/GRCh38#14239680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

14239703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

14239854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

http://identifiers.org/hco/2/GRCh38#14239877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

14239933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

14240309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

14240866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585743-T-C

14240931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585678-C-T

http://identifiers.org/hco/2/GRCh38#14240954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14585655-C-A

14241015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585598-A-T

14241339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585323-A-G

14241349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585308-T-C

14241404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585277-A-G

14241404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585277-A-T

14241542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585160-T-G

14241674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14585022-A-G

14241913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14584788-G-A

14241971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14584730-C-T

http://identifiers.org/hco/2/GRCh38#14241972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14584729-C-A

14260165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14569197-A-G

14260228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14569134-T-C

14260235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14569127-G-A

14260329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14569045-G-A

14260609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568774-A-G

14260723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568688-A-G

14260783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568630-A-G

14260905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568521-T-A

14260905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568521-T-G

14260944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568386-A-G

14260948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568382-T-A

14261129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568134-C-T

14261220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14568075-C-T

14261461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14567843-C-T

14261601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14567716-T-C

14261757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14567565-A-G

http://identifiers.org/hco/2/GRCh38#14261887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14567393-C-A

14263956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14565928-A-G

14264061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14565821-T-A

14266784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564448-T-C

14266784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564448-T-G

14266790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564442-A-G

http://identifiers.org/hco/2/GRCh38#14266980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14564268-A-C

14267084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564170-T-A

http://identifiers.org/hco/2/GRCh38#14267105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14564149-C-A

14267126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564128-C-T

14267202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564052-C-G

14267202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14564052-C-T

14268456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563785-A-G

http://identifiers.org/hco/2/GRCh38#14268505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14563751-C-A

14268526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563738-G-A

14268570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563695-T-G

14268602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563683-C-G

14268607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563678-T-A

http://identifiers.org/hco/2/GRCh38#14268639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14563646-A-C

14268671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563616-A-T

14268727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14563550-G-A

14269723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14552702-C-T

14269841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14552580-T-A

14269923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14552497-T-C

http://identifiers.org/hco/2/GRCh38#14269950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14552470-A-C

14270581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14552326-A-T

http://identifiers.org/hco/2/GRCh38#14270615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14552291-A-C

14270631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14552275-G-C

14270747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14551773-A-G

14270881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14551652-A-G

14270912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14551621-A-T

http://identifiers.org/hco/2/GRCh38#14270926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14551607-C-A

14270926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14551607-C-G

14273213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14538543-G-A

14273262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14538501-A-G

14273285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14538478-G-C

14273305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14538470-T-C

http://identifiers.org/hco/2/GRCh38#14273492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14538271-C-A

14273671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14538094-T-C

14273966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537618-G-A

14274015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537566-A-G

14274021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537560-T-C

14274021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537560-T-G

14274108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537477-T-C

14274108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537477-T-G

14274118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537467-C-G

14274404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14537228-T-C

http://identifiers.org/hco/2/GRCh38#14274461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14537175-A-C

14275160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535671-G-A

14275168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535663-C-T

14275193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535638-C-G

14275338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535501-T-G

14275418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535353-A-G

14275429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535342-T-A

14275517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535191-T-C

14275544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535165-C-G

14275584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535117-A-G

14275658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535042-T-A

14275658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535042-T-C

14275686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14535021-T-A

http://identifiers.org/hco/2/GRCh38#14275869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14534877-C-A

14275913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14534829-A-G

14276856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14534524-G-A

14277038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14534285-T-C

14279704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14533743-T-A

14279874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14533584-C-G

http://identifiers.org/hco/2/GRCh38#14280049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14532882-A-C

14280113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532808-A-G

14280133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532788-G-A

http://identifiers.org/hco/2/GRCh38#14280143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14532776-C-A

14280143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532776-C-G

14280143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532776-C-T

http://identifiers.org/hco/2/GRCh38#14280164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14532755-C-A

14280164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532755-C-T

14280258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532679-T-A

http://identifiers.org/hco/2/GRCh38#14280321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14532616-A-C

14280419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532520-C-T

14280649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532313-T-C

14281038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532155-A-G

14281057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532136-T-C

14281195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14532008-T-C

14281469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14531735-G-T

14281603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14531615-G-A

http://identifiers.org/hco/2/GRCh38#14281632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14531587-C-A

14281689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14531529-T-C

14281730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14531493-G-T

14283362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14530123-A-G

14283378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14530106-T-A

14283378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14530106-T-C

14283648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14529856-A-T

http://identifiers.org/hco/2/GRCh38#14283663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14529838-C-A

14283663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14529838-C-T

14283917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14529124-T-A

14283921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14529120-C-T

14284103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528942-G-A

14284103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528942-G-T

14284308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528756-A-G

14284356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528707-A-G

14284356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528707-A-T

http://identifiers.org/hco/2/GRCh38#14284362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14528701-C-A

14284362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528701-C-T

14284489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528573-A-G

14284553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528505-C-T

14284690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528390-G-A

14284706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528375-C-T

14284731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528331-A-T

14284860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528207-G-A

14284929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528138-T-C

14284929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14528138-T-G

http://identifiers.org/hco/2/GRCh38#14284970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14528097-A-C

14285066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527996-C-T

14285157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527905-G-A

http://identifiers.org/hco/2/GRCh38#14285272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14527793-C-A

14285324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527742-A-G

14285357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527709-T-C

14285363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527703-G-C

14285383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527679-A-T

14285602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527470-C-T

http://identifiers.org/hco/2/GRCh38#14285703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14527376-A-C

14285703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14527376-A-G

http://identifiers.org/hco/2/GRCh38#14285863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14527214-A-C

14286058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14526979-T-A

14286080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14526942-G-A

14286103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14526919-A-G

14286149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14526878-C-T

14288609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523721-A-G

14288749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523580-G-A

14288856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523468-A-T

14288868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523456-A-G

http://identifiers.org/hco/2/GRCh38#14288898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14523434-C-A

14288916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523420-A-G

14288916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523420-A-T

14288930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523404-C-G

14289042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523288-T-C

14289330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523044-G-A

14289385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14523011-C-T

14289526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522906-C-T

14289547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522885-G-A

14289855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522628-A-G

14290027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522479-T-C

14290033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522473-C-T

http://identifiers.org/hco/2/GRCh38#14290048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14522458-C-A

14290076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522429-C-T

14290129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522337-A-G

14290176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522291-T-C

14290183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522284-G-T

14290243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522224-A-G

14290456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14522042-T-C

14290495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521992-G-C

14290521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521958-G-C

14290596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521892-G-A

14290596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521892-G-C

http://identifiers.org/hco/2/GRCh38#14290735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14521771-A-C

14290869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521650-G-T

14291097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521450-C-T

14291193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521365-C-G

14291222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521334-A-G

http://identifiers.org/hco/2/GRCh38#14291224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14521332-C-A

14291443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521138-A-G

14291456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521126-A-G

14291518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521065-A-G

14291551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521032-T-C

14291569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14521018-T-C

http://identifiers.org/hco/2/GRCh38#14291764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14520866-C-A

http://identifiers.org/hco/2/GRCh38#14291840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14520792-A-C

14292866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518815-T-C

14292871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518810-A-G

14292935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518747-G-A

14292954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518720-A-T

14293013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518669-A-G

14293047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518635-C-T

14293101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518583-T-G

14293129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518553-A-G

14293131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518551-A-G

14293147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518534-C-G

14293159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518522-C-T

14293245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518428-G-A

14293263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518410-T-C

14293294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518379-G-T

14293303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518370-T-C

14293361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518304-T-C

14293425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14518240-C-T

http://identifiers.org/hco/2/GRCh38#14293453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14518212-C-A

14293518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14517288-A-G

14293663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14517146-A-G

14293787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14517021-A-G

14293787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14517021-A-T

14293815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14516996-G-A

14293831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14516980-G-C

http://identifiers.org/hco/2/GRCh38#14294019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14516786-C-A

14296111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14514746-T-C

14296227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14514640-T-A

http://identifiers.org/hco/2/GRCh38#14296307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14514575-C-A

14296634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14514326-T-G

14296764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14514214-A-G

14296967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14514021-T-A

14297079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513909-G-A

14297093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513897-T-A

14297120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513874-A-T

14297134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513853-T-C

14297408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513319-G-A

14297419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513308-T-A

14297419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14513308-T-G

14298030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14512711-C-G

14298555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511962-G-T

14298594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511925-T-A

14298610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511910-A-G

14298958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511515-G-C

14299004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511470-A-G

14299141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511351-T-A

14299141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14511351-T-C

14299761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510752-C-T

14299859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510650-G-A

14299913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510601-T-C

14299935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510579-G-A

http://identifiers.org/hco/2/GRCh38#14300003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14510515-C-A

14300016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510502-T-C

14300133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14510216-A-G

14300456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509971-T-A

14300456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509971-T-G

14300544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509883-T-C

14300763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509680-T-C

14300763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509680-T-G

14300834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509614-T-A

14300834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509614-T-C

14300860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509588-T-C

14301018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509437-G-C

14301919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509314-T-G

14302095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509145-T-C

14302184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14509058-C-T

14302250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14508991-T-C

14302369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14508875-C-T

14302520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14508807-A-G

14302520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14508807-A-T

14302802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14498829-T-A

http://identifiers.org/hco/2/GRCh38#14302933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14498702-A-C

14302961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14498673-C-T

14303002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14498632-G-C

http://identifiers.org/hco/2/GRCh38#14303087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14498547-A-C

14303229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14498403-A-G

14303493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497853-G-A

http://identifiers.org/hco/2/GRCh38#14303544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14497802-A-C

14303544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497802-A-G

14303650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497702-G-A

14303650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497702-G-T

14303659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497691-A-G

14303679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497671-C-G

14303688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497662-T-C

14303705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497645-T-C

14303729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497619-G-A

14303729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497619-G-T

14304004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497343-T-G

14304035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497314-A-G

14304072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497283-G-T

14304077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497278-G-T

14304096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497259-A-G

14304159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497227-T-C

14304224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497179-T-A

14304411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497013-T-C

14304418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497011-C-G

14304418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14497011-C-T

14304463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14496967-A-G

14304617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14496827-T-C

14304670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14496774-T-A

14306642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14496147-A-T

14306685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14496110-A-G

14307064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495718-T-C

14307362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495381-T-G

14307501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495237-T-C

14307507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495231-T-C

14307693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495053-G-A

14307694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14495052-C-T

14307825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494837-A-G

14307853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494809-A-G

http://identifiers.org/hco/2/GRCh38#14307875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14494787-C-A

14307889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494773-A-G

http://identifiers.org/hco/2/GRCh38#14307905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14494761-A-C

14307940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494726-G-C

14307996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494668-C-T

14308045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494617-G-A

14308054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494608-C-G

14308055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494606-T-C

14308055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494606-T-G

14308106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494556-C-T

14308910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14494137-G-C

14309042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14490304-G-A

14309042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14490304-G-T

14309093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14490266-C-G

14309140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14490222-G-A

http://identifiers.org/hco/2/GRCh38#14309149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14490214-C-A

http://identifiers.org/hco/2/GRCh38#14309239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14490126-A-C

14309239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14490126-A-G

http://identifiers.org/hco/2/GRCh38#14309840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14489823-A-C

14309896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489765-A-G

14309909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489752-A-G

http://identifiers.org/hco/2/GRCh38#14309943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14489721-C-A

14309943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489721-C-T

http://identifiers.org/hco/2/GRCh38#14310350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14489579-C-A

14310350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489579-C-T

14310669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489292-C-T

14310742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489212-A-T

14310778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489176-T-A

14310879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489079-T-G

14310918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14489039-G-A

http://identifiers.org/hco/2/GRCh38#14310956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14489000-C-A

14310972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488984-A-T

14313023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488276-T-C

14313023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488276-T-G

14313034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488269-A-T

14313053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488250-T-A

14313190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488129-G-A

14313231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14488088-A-T

14313324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487997-C-T

14313411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487910-T-C

14313512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487803-T-A

14313636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487679-T-C

14313733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487582-G-A

14313733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487582-G-T

14314170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487207-G-A

http://identifiers.org/hco/2/GRCh38#14314206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14487171-A-C

14314340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14487049-G-T

14314568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486815-T-C

http://identifiers.org/hco/2/GRCh38#14314696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14486703-A-C

14314705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486694-G-A

14314882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486532-G-A

14314973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486412-C-T

14314997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486389-G-A

14315021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486365-T-C

http://identifiers.org/hco/2/GRCh38#14315053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14486333-A-C

14315131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486260-T-A

14315153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14486237-C-T

14315585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14485523-G-T

http://identifiers.org/hco/2/GRCh38#14315591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14485517-C-A

14315628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14485480-G-T

14315692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14485415-T-A

14315692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14485415-T-C

14316057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14485047-C-G

14316306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484778-A-G

http://identifiers.org/hco/2/GRCh38#14316487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14484618-A-C

14316520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484594-C-T

14316815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484304-G-A

http://identifiers.org/hco/2/GRCh38#14316892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14484230-C-A

14316892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484230-C-T

14316944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484181-C-T

14317023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14484105-A-G

14317075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14484068-T-C

14317095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14484048-G-A

14317095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14484048-G-T

14317126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484027-G-A

14317143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14484010-A-G

14318381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14480354-T-C

14318580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14479350-G-A

14318843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14479090-G-C

14318907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478977-A-G

14318931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478949-A-G

14318956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478924-A-G

14319061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478828-G-C

14319116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478778-A-G

14319140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478756-A-T

14319144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478752-G-A

14319193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478703-A-G

14319194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478702-T-G

14319651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478258-G-A

14319655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478254-T-C

14320610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14478052-G-T

14320783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14477901-A-G

14320795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14477889-G-A

14320995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14477721-C-T

14321128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14477575-T-G

14321187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14477544-G-A

http://identifiers.org/hco/2/GRCh38#14322767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14476813-C-A

14322827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476752-T-G

14322855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476427-C-G

14323008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476261-A-T

14323056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476214-T-G

14323118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476151-G-A

14323209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14476056-T-C

http://identifiers.org/hco/2/GRCh38#14323276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14475989-C-A

14323396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475926-T-A

14323742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475641-A-G

14323820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475573-T-A

14323857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475542-G-A

14323913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475407-C-T

14324081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475235-T-G

14324273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475060-T-A

14324278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475055-G-A

14324278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14475055-G-C

14324412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474932-T-C

14324445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474898-A-G

14324588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474757-A-G

http://identifiers.org/hco/2/GRCh38#14324641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14474703-C-A

http://identifiers.org/hco/2/GRCh38#14324661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14474683-A-C

14324665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474679-C-T

14324735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474604-C-T

http://identifiers.org/hco/2/GRCh38#14324744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14474595-A-C

14324744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474595-A-T

14324791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474548-A-G

14324930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474442-G-A

14325010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474370-G-A

14325035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474347-G-A

14325061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474322-G-A

14325413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474040-T-C

14325538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14474006-T-A

14325556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14473988-G-A

http://identifiers.org/hco/2/GRCh38#14325570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14473974-C-A

http://identifiers.org/hco/2/GRCh38#14325591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14473953-C-A

14325624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14473920-A-G

14325766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14473794-A-G

http://identifiers.org/hco/2/GRCh38#14329035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14466849-A-C

14329035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14466849-A-G

14329151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14466734-A-G

14329279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14466622-G-T

14329607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14466228-C-T

14330102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14465854-A-G

14330389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14465592-T-C

14330808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14464765-A-G

14330892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14464693-G-A

14330961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14464623-G-A

14330961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14464623-G-C

14330994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 14464586-C-T

14346667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462736-G-T

14347071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462451-T-A

http://identifiers.org/hco/2/GRCh38#14347200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14462327-A-C

14347232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462300-T-G

http://identifiers.org/hco/2/GRCh38#14347300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14462250-C-A

14347300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462250-C-T

14347357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462195-G-A

14347399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462153-T-C

14347420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14462129-A-T

14347563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461992-C-T

14347627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461928-T-C

http://identifiers.org/hco/2/GRCh38#14347633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14461922-C-A

14347638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461917-T-C

14347661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461880-G-A

14347706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461835-T-C

http://identifiers.org/hco/2/GRCh38#14347760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14461783-C-A

14347815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461721-A-G

14347868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461661-G-T

14348493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461330-G-A

14348552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461270-C-T

14348790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14461055-G-C

14348893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460966-G-A

14348893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460966-G-C

14348897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460962-A-G

14349067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460829-A-G

14349333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460436-A-G

14349499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460285-T-C

14349959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460198-T-G

14349969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14460188-A-G

14350379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14459704-T-C

14350381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14459702-T-A

14351318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14456198-C-T

14351558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455986-A-G

14351649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455911-T-C

14351706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455857-G-A

14352050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455541-T-G

14352331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455294-A-G

14352368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14455257-A-G

14352989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14454583-T-C

14353298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453919-T-A

14353309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453908-C-G

14353362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453856-A-G

14353413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453801-T-A

http://identifiers.org/hco/2/GRCh38#14353684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14453539-C-A

14353684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453539-C-T

http://identifiers.org/hco/2/GRCh38#14353743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14453458-A-C

14354736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14453194-A-G

14355086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14451037-T-C

14355240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14450884-C-G

http://identifiers.org/hco/2/GRCh38#14357181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14433470-C-A

14357184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14433467-T-G

14357185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14433466-G-A

http://identifiers.org/hco/2/GRCh38#14357325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14433329-C-A

14357465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14433190-C-T

14357880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14432729-G-A

14357914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14432689-C-G

14357955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14432656-G-C

14358143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14432437-A-G

14363382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14426252-T-C

http://identifiers.org/hco/2/GRCh38#14363411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14426224-C-A

14363495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14426140-C-T

14363550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14426089-C-T

http://identifiers.org/hco/2/GRCh38#14363771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14425876-C-A

14366431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14425312-A-T

14366692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14425067-T-G

14366739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14425020-T-C

14366798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424996-A-G

http://identifiers.org/hco/2/GRCh38#14367150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14424679-C-A

14367152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424677-G-A

14367205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424596-T-A

14367207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424594-A-G

14367572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424237-T-G

14367618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14424190-C-T

14367740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423843-G-A

14367870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423706-T-A

14367938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423653-T-C

14368033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423554-T-C

14368147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423487-T-C

14368301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14423342-A-G

14373786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14420549-A-T

http://identifiers.org/hco/2/GRCh38#14373849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14420483-A-C

14373849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14420483-A-G

14384054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14413247-T-C

14384373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412944-A-G

14384429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412897-C-G

14384696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412655-T-C

14384718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412633-T-C

14384720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412631-T-C

14384925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412471-G-C

14385194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412239-A-T

http://identifiers.org/hco/2/GRCh38#14385290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14412147-A-C

14385319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412118-T-C

14385354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412081-C-T

14385408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412015-C-T

14385412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14412011-T-G

14385517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14411949-G-A

14385557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14411906-T-C

14385589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14411877-T-G

14385668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14411799-C-T

14385933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14411497-C-T

14392597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14402032-T-C

14392990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14401660-G-A

14393017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14401634-G-A

http://identifiers.org/hco/2/GRCh38#14393045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14401596-C-A

14393045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14401596-C-G

14393876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400799-A-G

14393876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400799-A-T

14394026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400649-G-C

14394272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400401-T-C

14394276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400397-T-A

http://identifiers.org/hco/2/GRCh38#14394359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14400310-A-C

14394631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14400049-G-C

14394849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399784-C-T

14394855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399781-G-A

14394924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399724-G-C

14394981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399649-C-T

14395054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399562-A-G

http://identifiers.org/hco/2/GRCh38#14395092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14399524-C-A

14395108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14399508-T-A

http://identifiers.org/hco/2/GRCh38#14395177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14399402-A-C

14395516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14398861-C-G

14395558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14398820-C-G

14396424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14397494-C-T

14396613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14397303-C-G

14396613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14397303-C-T

14396621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14397295-C-T

14397025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396857-A-T

14397104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396779-C-T

14397265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396652-C-T

14397315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396600-T-C

14397331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396584-A-G

14397416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396503-C-T

14397423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396496-G-T

14397458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396461-T-C

14397548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396386-A-G

14397566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396373-G-A

14397711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396237-C-T

http://identifiers.org/hco/2/GRCh38#14397712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14396236-A-C

14397712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14396236-A-G

14397900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14393388-T-C

14398116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14393169-G-T

14398260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14393037-T-A

14398493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392797-T-C

14398500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392790-G-T

14398502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392788-G-C

14398559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392731-G-T

http://identifiers.org/hco/2/GRCh38#14398569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14392721-C-A

14398611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392679-G-C

14398857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392220-C-T

14398932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14392053-A-G

http://identifiers.org/hco/2/GRCh38#14398938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14392047-C-A

14399078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14391912-C-T

14399100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14391891-T-G

14399101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14391890-T-C

14399354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14391680-G-A

14400318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14390643-A-G

14400330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14390624-G-A

14400644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14390327-A-T

14400775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14390207-T-C

http://identifiers.org/hco/2/GRCh38#14400890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14389737-C-A

http://identifiers.org/hco/2/GRCh38#14400929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#14389705-C-A

14400929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14389705-C-T

14400939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38663
most severe consequence: non coding transcript exon variant
orthologous variants: 14389695-T-C