http://identifiers.org/hco/12/GRCh38#71938896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#115020873-A-C

71938896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 115020873-A-G

71939065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 115020714-G-A

http://identifiers.org/hco/12/GRCh38#71939184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115020597-C-A

71939184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020597-C-T

71939210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020573-A-G

71939341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020467-T-G

71939371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020437-G-A

71939371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020437-G-T

71939387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020421-T-A

71939645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020222-A-T

71939697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115020171-C-T

71940015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019818-A-G

71940033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019800-T-C

71940230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019604-A-T

71940243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019591-G-C

71940243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019591-G-T

71940727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115019188-A-G

http://identifiers.org/hco/12/GRCh38#71941448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115018927-C-A

71941448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018927-C-T

71941466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018909-T-A

71941490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018885-G-C

71941490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018885-G-T

71941537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018839-G-T

71941671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115018721-G-A

71941738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115018654-A-G

71942661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115017361-C-T

71943089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016951-T-G

71943156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016882-A-G

71943375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016781-T-G

71943376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016780-G-A

71943397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016760-G-A

71943397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016760-G-T

71943488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016675-C-T

http://identifiers.org/hco/12/GRCh38#71943593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115016563-C-A

71943812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115016367-T-C

71943947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015947-A-G

71943979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015911-C-T

http://identifiers.org/hco/12/GRCh38#71944059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115015823-C-A

71944063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015819-C-T

71944096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015788-A-G

http://identifiers.org/hco/12/GRCh38#71944151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115015747-C-A

http://identifiers.org/hco/12/GRCh38#71944169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115015727-C-A

71944169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015727-C-T

71944193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015710-T-C

71944197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015706-G-C

71944197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015706-G-T

http://identifiers.org/hco/12/GRCh38#71944246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115015661-C-A

71944246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015661-C-G

71944266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015640-T-C

71944318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015585-A-G

71944328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015575-G-T

71944336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015567-C-T

71944363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015540-T-A

71944563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015348-T-G

71944657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015254-T-A

71944657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115015254-T-C

71944740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015182-G-T

http://identifiers.org/hco/12/GRCh38#71944809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115015113-A-C

71944809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015113-A-T

71944816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015106-G-A

71944842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115015080-C-T

71944929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115014993-G-A

71944929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115014993-G-C

71945004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115014918-G-A

http://identifiers.org/hco/12/GRCh38#71945176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115014750-C-A

71945762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013815-A-T

71945940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013646-A-G

71945953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013640-T-G

71945999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013595-C-T

71946076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013522-G-C

http://identifiers.org/hco/12/GRCh38#71946091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115013507-A-C

71946104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013494-A-G

71946358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013030-G-A

71946361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115013027-G-A

http://identifiers.org/hco/12/GRCh38#71946421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115012965-A-C

71946563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012818-G-C

71946623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012757-T-C

71946623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012757-T-G

71946735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012638-G-A

71946735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012638-G-T

71947042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012340-A-G

71947254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012189-G-C

71947292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115012150-G-A

71947703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011808-C-T

71947749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115011762-T-C

71947755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115011738-G-A

71947857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115011634-G-A

71947965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115011528-T-C

71948073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115011418-C-T

71948204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011371-T-A

71948289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011289-A-G

71948302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011274-A-G

71948391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011206-C-T

71948557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115011047-C-T

71948611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010993-G-A

71948731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010891-T-C

71948777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010834-A-G

71948825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010788-A-G

71948892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010726-G-T

http://identifiers.org/hco/12/GRCh38#71949059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115010539-A-C

71949059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010539-A-G

71949059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010539-A-T

71949210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010405-A-G

71949297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010317-A-T

71949313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010301-C-T

71949372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010241-G-A

71949434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010180-A-G

http://identifiers.org/hco/12/GRCh38#71949449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115010164-C-A

71949457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115010156-T-C

71949668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009942-A-G

http://identifiers.org/hco/12/GRCh38#71949705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115009904-C-A

71949705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009904-C-T

71949772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009837-T-A

71949880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009741-T-A

71949978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009650-A-G

71950094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009533-C-T

71950143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009481-A-T

71950215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009428-A-G

71950752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009167-C-T

71950808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009112-G-A

71950868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115009069-T-C

http://identifiers.org/hco/12/GRCh38#71950929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115008969-A-C

71951344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008588-G-A

71951353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008579-G-A

71951362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008564-G-A

71951369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008555-G-A

http://identifiers.org/hco/12/GRCh38#71951379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115008545-C-A

71951422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008502-C-T

71952285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008045-T-C

71952314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115008006-A-G

71952355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115007965-A-G

71952738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115007610-G-A

71952739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115007609-C-T

71953137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115007340-A-G

http://identifiers.org/hco/12/GRCh38#71953184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115007291-A-C

71953429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006756-T-G

71953431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006754-G-A

71953854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006021-A-G

71953857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115006018-A-T

71954034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005836-T-C

71954385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005452-G-A

71954385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005452-G-T

http://identifiers.org/hco/12/GRCh38#71954480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115005364-C-A

71954484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005354-T-G

71954549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005299-G-A

71954573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005251-G-A

71954716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005114-A-G

71954742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115005090-G-C

71954855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004959-T-C

71954921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004897-A-T

71954939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004879-T-C

http://identifiers.org/hco/12/GRCh38#71955014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115004808-A-C

71955120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004703-C-T

71955153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004671-C-G

71955153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004671-C-T

71955400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115004119-A-G

71955612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003959-A-G

71955800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003846-C-T

71955841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003807-C-T

71955891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003751-T-A

71955960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115003671-T-C

71956018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003630-G-A

71956074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003575-A-T

71956085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115003565-T-C

http://identifiers.org/hco/12/GRCh38#71956141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115003509-C-A

71956977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002760-A-T

71957228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002344-A-T

71957311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002244-T-C

71957325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002230-G-A

71957325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002230-G-C

71957325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115002230-G-T

71958178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999182-A-G

71958248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999112-T-C

71958248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999112-T-G

http://identifiers.org/hco/12/GRCh38#71958326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115000963-C-A

71958682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000596-A-G

http://identifiers.org/hco/12/GRCh38#71958699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#115000585-A-C

71959060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115000218-G-A

71959407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999880-T-C

71959435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999854-G-A

71959738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999551-G-A

http://identifiers.org/hco/12/GRCh38#71960265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114999043-C-A

71960276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114999014-G-A

71960374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998922-G-A

http://identifiers.org/hco/12/GRCh38#71960536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114998739-C-A

71960562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998713-G-C

71960575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998700-T-G

71960613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998653-G-C

71960692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998575-A-G

71960693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998574-C-T

71961115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998177-G-C

71961122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114998170-G-C

71961319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114997653-T-C

71961435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114997541-T-C

71961471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114997508-G-A

71961479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114997500-T-C

71961479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114997500-T-G

71961546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114997424-A-T

71961574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997401-T-C

71961621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997350-G-A

71961621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997350-G-C

71961650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997327-C-T

71961651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997326-A-G

71961748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997229-G-A

71961901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997078-A-G

71961945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997033-G-T

71961968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114997010-G-A

71962000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114996978-T-C

http://identifiers.org/hco/12/GRCh38#71962002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114996976-C-A

71962147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114996842-T-C

71962267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114996739-T-C

71962509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114996508-T-A

71963232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114995162-T-C

71963351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114995050-A-T

71966461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114994479-G-A

71966603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114994330-A-T

71966653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114994273-C-T

71967192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114993716-T-C

71967297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992813-A-G

71967445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992674-T-C

71967451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992668-C-T

71967452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992667-G-A

71967571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992570-T-G

71967651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992491-T-C

71967900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992231-G-T

71967913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114992218-T-C

http://identifiers.org/hco/12/GRCh38#71968475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114991617-C-A

71968494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114991595-C-T

71969678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114990376-T-C

71969819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114990266-T-C

71969883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114990220-T-C

http://identifiers.org/hco/12/GRCh38#71969943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114990166-A-C

71970297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114989829-G-A

http://identifiers.org/hco/12/GRCh38#71970923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114989237-C-A

71971396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988775-A-G

71971641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988401-G-A

71971852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988201-A-G

71971913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988143-T-G

71971937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988119-T-A

71971937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988119-T-C

71971938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988118-G-T

71972032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114988033-C-G

http://identifiers.org/hco/12/GRCh38#71972222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114987854-A-C

71972346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987364-C-T

71972373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987338-T-C

71972387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987331-T-A

71972387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987331-T-G

71972401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987317-T-A

http://identifiers.org/hco/12/GRCh38#71972416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114987302-C-A

71972416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987302-C-T

71972435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987270-G-A

71972435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987270-G-T

71972485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987219-G-A

71972485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114987219-G-T

71972520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 114987183-G-T

71972572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: 114987131-G-A

71972604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: 114987099-C-G

71972604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: 114987099-C-T

http://identifiers.org/hco/12/GRCh38#71972676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114987027-A-C

71972727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986978-C-T

71972755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986950-C-T

71972843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986865-G-A

71972843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986865-G-T

71972847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986861-A-G

71972855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986853-C-T

71972856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114986852-T-A

71972856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114986852-T-C

71972856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114986852-T-G

71974460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986180-C-G

71974511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986131-T-A

71974511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114986131-T-G

71974709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114985870-C-T

71974797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114985624-C-T

71975767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114984526-G-A

71976487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114984085-A-G

71976540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114984031-C-T

71976597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114983977-T-C

http://identifiers.org/hco/12/GRCh38#71978368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114982804-A-C

71978437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114982737-A-G

71978900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114982079-C-T

71979097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981884-T-A

71979118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981853-A-T

71979126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981845-A-T

http://identifiers.org/hco/12/GRCh38#71979266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114981736-C-A

71979266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981736-C-T

71979310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981695-T-G

71979587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981443-C-T

71979678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981344-C-T

71979738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981284-A-G

71979913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981116-T-C

71979916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114981113-T-A

71980311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114980748-C-G

71980427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114980631-G-A

71980820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114980235-G-A

71981233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114979827-T-C

71981335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114979740-T-G

71981469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, undefined
orthologous variants: 114979608-C-T

71981501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114979591-G-A

71981516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114979575-G-A

71982347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114977936-T-A

71982419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114977884-T-C

71982460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114977843-T-A

71983118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114974327-T-G

71983386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114974062-A-G

71983498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114973951-G-A

71983620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114973844-T-A

71983620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114973844-T-C

71984169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968852-A-G

71984182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968835-T-C

71984394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968485-A-G

71984533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968332-C-G

71984557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968306-C-G

71984557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968306-C-T

71984590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114968142-C-T

71984709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967978-T-G

71984817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967882-A-G

71984944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967482-C-G

71985245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967200-C-G

71985245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967200-C-T

71985802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114967009-T-C

http://identifiers.org/hco/12/GRCh38#71986112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114966790-C-A

71986260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966644-C-T

71986360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966544-C-G

71986361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966543-T-C

71986478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966421-A-G

71986517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966381-G-A

71986527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966371-A-T

71986686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966223-C-G

71986687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966222-T-A

71986813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114966088-T-A

http://identifiers.org/hco/12/GRCh38#71987093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114965799-A-C

71987422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114965494-G-T

http://identifiers.org/hco/12/GRCh38#71987898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114965333-C-A

71987987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114965243-T-C

71988033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114965198-G-C

71989180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114962434-G-A

71989311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114962174-C-G

71989453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114962038-C-T

71989584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961900-A-T

71989590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961894-A-G

71989590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961894-A-T

71989595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961889-T-A

http://identifiers.org/hco/12/GRCh38#71989764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114961715-C-A

71989834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961643-A-G

71989851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961626-G-T

71989952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961500-T-C

71990015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961444-C-T

71990210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961229-A-G

71990289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114961153-G-A

71990543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114960713-A-G

71990583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114960639-T-C

http://identifiers.org/hco/12/GRCh38#71990696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114960522-A-C

71990754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114960457-G-T

71990858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114960366-A-G

71991471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114959721-A-G

71991661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114959547-C-T

http://identifiers.org/hco/12/GRCh38#71991818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114959412-A-C

71991818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114959412-A-G

http://identifiers.org/hco/12/GRCh38#71991853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114959378-A-C

71992125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114959066-A-G

71993290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114958155-G-A

71993426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114958017-T-A

http://identifiers.org/hco/12/GRCh38#71993543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114957900-C-A

71993584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114957859-G-C

71993757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114957692-C-G

http://identifiers.org/hco/12/GRCh38#71994342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114955963-C-A

71994342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955963-C-T

71994357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955942-A-G

71994369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955930-A-T

71994521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: 114955772-G-A

71994590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955697-C-G

71994627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955668-T-C

71994703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955599-T-C

71994843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955458-A-G

71995099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955198-A-G

71995099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955198-A-T

71995163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114955139-G-A

71995351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114954968-C-T

71997636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953998-T-C

71998126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953350-T-G

71998132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953337-G-A

71998138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953331-G-A

71998377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953100-C-T

71998379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953098-G-A

71998434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114953047-T-C

71998524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952959-A-G

71998524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952959-A-T

71998675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952834-G-T

71998910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952605-G-A

71998910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952605-G-T

71999017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952497-A-G

71999146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952374-G-A

71999148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952372-G-A

71999313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114952205-T-C

71999710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114951816-T-C

71999738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114951788-A-G

71999738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114951788-A-T

http://identifiers.org/hco/12/GRCh38#71999747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114951779-A-C

71999802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114951728-G-T

http://identifiers.org/hco/12/GRCh38#71999868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114951662-C-A

71999868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114951662-C-G

72000658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114949805-T-C

72000744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114949741-T-G

72000936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114949567-T-C

72001204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114949289-A-G

72001728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114949041-T-G

72002650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948780-C-T

72002678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948755-G-A

72002723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948706-T-C

72002774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948670-G-T

72002794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948650-T-A

72002794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948650-T-C

72003125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114948327-T-C

72003781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114947747-C-T

72004378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114946915-T-C

72004469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114946839-T-A

http://identifiers.org/hco/12/GRCh38#72004588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114946724-C-A

http://identifiers.org/hco/12/GRCh38#72004996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114946331-C-A

72005055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114946272-G-A

72005055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114946272-G-C

72005123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114946204-A-G

72005591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114945498-T-A

72005764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114945332-T-C

72005783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114945331-T-G

72005842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114945296-C-T

72005961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114945056-G-T

72006529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114944565-G-A

72007104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114944095-T-A

72007352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943841-G-A

72007377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943816-A-G

72007431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943766-T-C

72007574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943622-A-T

72007762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943215-G-T

72007858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943121-G-C

72007858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114943121-G-T

72009525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114942528-T-C

72009607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114942446-A-G

72009628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114942426-T-C

http://identifiers.org/hco/12/GRCh38#72009995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114942107-A-C

72009995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114942107-A-G

72010116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114941984-A-G

72010311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114941794-T-A

72010539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114941579-A-G

72010540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114941578-T-C

72010560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114941551-T-C

http://identifiers.org/hco/12/GRCh38#72010899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114941212-A-C

72011306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940753-T-C

http://identifiers.org/hco/12/GRCh38#72011432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114940628-A-C

72011655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940385-C-T

http://identifiers.org/hco/12/GRCh38#72011742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114940300-C-A

72011742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940300-C-G

72011742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940300-C-T

72011814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940222-T-G

72011841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940196-G-A

72011889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114940143-T-A

72012079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114939926-A-T

72012207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114939834-C-T

72012276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114939771-A-G

72012284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114939763-A-G

http://identifiers.org/hco/12/GRCh38#72012710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114939284-C-A

72012710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114939284-C-G

72013105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114938844-T-A

72013238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114938712-G-A

72013238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114938712-G-C

72013312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114938642-C-T

72013655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114937813-G-A

72014775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114937275-A-G

72014932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114937075-G-A

72014932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114937075-G-C

72014932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114937075-G-T

72015010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936997-T-C

72015135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936863-G-A

72015263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936737-G-A

72015747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936597-C-T

72015754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936590-T-C

72015754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936590-T-G

72015769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936575-C-T

72015847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936500-G-A

72015866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936481-A-G

72015918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114936428-C-T

72015998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114935882-T-G

72016060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114935819-A-G

72016489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114935433-G-T

http://identifiers.org/hco/12/GRCh38#72017163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114933346-C-A

72017399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114933117-A-G

72017422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114933094-T-G

72017588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932925-C-T

72017892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932606-G-A

72018139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932376-G-A

http://identifiers.org/hco/12/GRCh38#72018143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114932373-C-A

72018143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932373-C-T

http://identifiers.org/hco/12/GRCh38#72018290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114932229-A-C

72018297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932222-C-T

72018351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932166-G-C

72018449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114932067-C-T

72018648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114931868-T-C

72019003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114931500-A-G

72019119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114931394-C-T

72019171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114931343-A-T

72019197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114931317-C-T

72021000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114928468-A-G

72021997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114927228-T-G

72022052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114927172-T-C

72022124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114927096-A-T

72022210-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114927012-A-T

72022379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926744-A-T

72022414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense variant
orthologous variants: 114926685-A-G

http://identifiers.org/hco/12/GRCh38#72022520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114926579-C-A

72022520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926579-C-T

http://identifiers.org/hco/12/GRCh38#72022545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114926554-C-A

72022545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926554-C-T

72022549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926550-G-A

72022549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926550-G-T

72022581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926518-A-G

72022612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926488-G-A

72022734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926367-G-T

72022745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114926356-T-C

72023039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925880-A-G

72023278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925691-A-G

http://identifiers.org/hco/12/GRCh38#72023311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114925659-A-C

72023312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925658-T-C

72023363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925607-T-C

72023376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925594-T-A

72023378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925592-A-G

72023494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925497-T-C

72023531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925463-T-C

72023971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925332-G-A

72024127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925190-G-A

72024220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114925107-C-T

72024553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114924144-A-G

72024728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114923976-G-A

72024910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114923794-A-G

72024956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114923748-A-G

http://identifiers.org/hco/12/GRCh38#72025022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114923683-A-C

72025141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114923388-G-T

72025313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114923260-G-C

72025663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114922683-G-A

72025723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114922624-G-A

72025763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114922584-T-C

72025795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114922552-T-C

72026550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114921454-T-C

72026607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114921398-A-T

72026814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114921204-T-A

72026969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114920881-A-T

72027271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114920554-C-T

72027272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114920553-C-G

72027718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114920271-T-C

http://identifiers.org/hco/12/GRCh38#72027773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114920225-C-A

72027911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114920105-G-T

72028321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114918971-A-G

72028434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114918877-T-C

72028730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114918596-G-T

72029097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114918009-G-A

72029129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917982-C-T

72029140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917971-T-C

72029145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917966-G-A

72029605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917504-G-A

72029614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917495-C-T

72029616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917493-A-G

72029620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917489-C-G

72029689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917427-T-C

72029711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917406-A-T

72029738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917364-T-C

72029811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917294-C-G

72029854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917251-G-A

72029906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917198-A-G

72030067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917095-G-A

72030171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114917023-T-C

72030409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916853-T-C

http://identifiers.org/hco/12/GRCh38#72031015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114916240-C-A

72031074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916179-A-T

72031106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916150-G-A

72031106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916150-G-T

http://identifiers.org/hco/12/GRCh38#72031138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114916120-C-A

72031138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916120-C-G

72031138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916120-C-T

72031197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916072-T-A

72031197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron variant
orthologous variants: 114916072-T-C

72031276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114915993-G-A

72031276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114915993-G-T

http://identifiers.org/hco/12/GRCh38#72031396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114915873-A-C

72031459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114915812-T-C

72031464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114915807-A-T

http://identifiers.org/hco/12/GRCh38#72031475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114915796-C-A

72031510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114915755-T-A

72031735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915529-G-C

72031735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915529-G-T

72031746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915517-G-C

http://identifiers.org/hco/12/GRCh38#72031885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114915387-C-A

72031885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915387-C-G

72031885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915387-C-T

72031924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915347-T-A

72031924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915347-T-C

72031969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915291-A-G

72032007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915255-T-C

72032011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915251-A-G

72032017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915237-G-T

72032034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915220-A-T

http://identifiers.org/hco/12/GRCh38#72032137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114915129-C-A

72032137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114915129-C-T

72032396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114914868-T-C

72032438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114914827-G-C

72032779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114914548-G-A

72032800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114914527-T-G

72033060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114914223-G-A

http://identifiers.org/hco/12/GRCh38#72033200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114911297-C-A

72033218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114911279-T-C

72033242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114911257-C-T

72033348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910934-G-A

72033723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910551-T-C

72033799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910457-A-T

72033843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910412-A-G

72034093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910154-G-A

72034175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910072-G-T

72034213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910034-T-C

72034238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114910009-G-A

72034782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114909268-T-C

72034876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114909169-G-C

72035018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114909021-C-T

72035050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908989-T-C

72035078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908960-T-C

72035078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908960-T-G

72035120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908917-G-A

72035178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908817-A-G

http://identifiers.org/hco/12/GRCh38#72035190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114908805-C-A

72035388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908622-G-A

72035388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114908622-G-T

http://identifiers.org/hco/12/GRCh38#72035761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114907372-C-A

72035973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114907195-A-G

72036010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114907159-T-C

72036073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114907130-G-A

72036113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114907097-T-C

72036174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114907036-G-C

72036374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906850-T-C

72036501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906729-A-G

72037031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906193-C-T

72037206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906018-T-A

72037215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906009-T-G

72037218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114906006-C-T

72037323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114905900-G-A

72037411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114905812-C-T

http://identifiers.org/hco/12/GRCh38#72041291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114903978-A-C

72042229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114899870-T-C

72042483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114899617-G-A

72043636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114897073-G-T

72043859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114896886-T-A

72044101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114896639-C-T

72044339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114896420-G-A

72044342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114896417-C-T

72044386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114896381-C-T

72044771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114894671-T-C

72044977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114894434-T-A

72045026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114894386-C-T

72045061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114894351-C-G

72045494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114893574-T-C

72045652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114893410-A-G

72045670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114893393-A-G

72046189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114892667-T-C

http://identifiers.org/hco/12/GRCh38#72046324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114892487-C-A

http://identifiers.org/hco/12/GRCh38#72046433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114892379-C-A

72046433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114892379-C-T

72046608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114892246-T-A

72046668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114892196-G-A

72048556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114891631-T-C

72048595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114891590-A-T

72049640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114889347-A-T

72049783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114889212-T-C

72049850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114889142-G-T

72049925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114889081-T-C

72050294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114888169-G-A

72050310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114888141-A-G

72050339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114888116-C-T

72050359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114888087-G-A

72050752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114887495-G-C

72050828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114887422-T-A

72051384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886548-C-T

72051568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886344-G-A

72051619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886304-A-G

72051652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886269-T-C

72051663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114886259-C-T

72052014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114885934-T-C

72052046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114885902-C-T

72052081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114885876-A-T

72053284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114884450-C-G

72053415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114884320-A-G

72053675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114884096-G-T

72053827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114883943-G-A

72053827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114883943-G-C

72053861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114883909-C-T

72054104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114883715-A-T

72054299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114883548-G-A

http://identifiers.org/hco/12/GRCh38#72054499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114882947-C-A

72054499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882947-C-T

72054699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882750-T-A

72054761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882689-T-C

72054822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882628-C-T

72054830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882620-C-T

http://identifiers.org/hco/12/GRCh38#72055053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114882466-A-C

72055062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882457-T-C

72055207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882332-C-T

72055255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882292-T-C

72055323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882221-T-C

http://identifiers.org/hco/12/GRCh38#72055333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114882208-A-C

72055333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882208-A-G

72055363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882169-C-T

72055376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882153-G-T

72055404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882125-C-T

72055457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882077-A-G

72055479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882055-T-C

72055488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114882051-T-C

72055541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881995-A-G

72055562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881984-T-G

72055861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881779-A-G

72055897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881746-A-G

72056079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881557-T-C

72056219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881421-A-G

72056219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881421-A-T

72056223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881415-A-T

72056296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881342-T-G

72056458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881193-C-T

72056532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114881124-G-A

72056657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880997-G-A

72056721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880933-C-T

72056855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880803-A-G

72057139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880332-A-T

72057232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880229-C-T

72057237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114880224-A-G

72057263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114880204-T-C

72057348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114880110-A-G

72057481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879978-T-C

72057520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879939-G-T

72057953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879528-C-T

72057963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879513-A-G

72058038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879453-T-A

http://identifiers.org/hco/12/GRCh38#72058054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114879436-C-A

72058054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879436-C-T

72058068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879422-A-G

72058096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114879412-G-A

72061256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114865136-T-C

http://identifiers.org/hco/12/GRCh38#72061687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114864705-C-A

72061702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864690-T-C

72061744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864647-G-A

72062111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864268-A-G

72062147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864232-G-C

72062217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864162-C-T

72062351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114864025-C-T

http://identifiers.org/hco/12/GRCh38#72062397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114863977-C-A

72062564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114863810-G-C

72062984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862874-C-T

72062993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862866-A-T

72063015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862844-G-A

72063042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862817-T-C

http://identifiers.org/hco/12/GRCh38#72063395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114862474-A-C

72063441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862428-A-G

72063870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114862028-T-C

72066492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861765-G-A

http://identifiers.org/hco/12/GRCh38#72066563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114861696-C-A

72066591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861668-G-C

72066676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861622-A-G

72066840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861549-A-T

72066896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861510-T-C

72066943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861464-G-A

72066980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861427-C-T

http://identifiers.org/hco/12/GRCh38#72066986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114861421-C-A

72067093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861318-C-T

72067225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114861187-T-C

http://identifiers.org/hco/12/GRCh38#72073118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114859396-A-C

72073257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114859208-C-T

72073374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114859083-T-C

72073452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858910-A-G

72073452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858910-A-T

72073563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858726-G-A

72073563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858726-G-T

72073577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858687-T-C

72073661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858598-C-T

72073672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858587-G-A

72073684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858575-T-C

72073686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858573-A-T

72073700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858555-T-A

72073700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114858555-T-C

72073730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858526-T-C

72073868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858418-T-C

72073975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114858311-T-C

http://identifiers.org/hco/12/GRCh38#72074163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114858126-A-C

72074333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857659-A-G

72074444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857471-T-G

72074454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857461-G-T

http://identifiers.org/hco/12/GRCh38#72074475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114857440-A-C

72074475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857440-A-G

http://identifiers.org/hco/12/GRCh38#72074652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114857292-A-C

72074735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857242-G-A

http://identifiers.org/hco/12/GRCh38#72074859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114857109-C-A

72074859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857109-C-G

72074990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114857000-A-T

72075045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114856943-A-G

72075168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114856829-G-A

72075179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114856818-T-C

72075188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114856809-C-G

72075481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114856125-T-C

72075481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 114856125-T-G

72075515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114856086-C-T

http://identifiers.org/hco/12/GRCh38#72075516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114856085-A-C

72075516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114856085-A-G

http://identifiers.org/hco/12/GRCh38#72075666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114855959-C-A

http://identifiers.org/hco/12/GRCh38#72075667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114855958-C-A

72075989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855667-A-G

72076030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855628-G-A

72076030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855628-G-C

72076366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855306-G-A

72076381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855291-G-C

72076442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855230-C-G

72076565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114855090-A-T

72076705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114854940-C-T

72077099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114854398-G-T

72077488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114854007-A-G

72077626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853868-T-G

72077662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853829-T-C

72077701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853792-C-T

72077706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853787-A-T

72077727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853766-C-T

72077851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853636-T-A

72077929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853567-C-T

72078061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114853461-C-T

http://identifiers.org/hco/12/GRCh38#72081221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114851895-C-A

72081221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114851895-C-G

72081223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114851893-A-G

72081376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114851759-G-C

72081405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114851732-A-G

72082120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114850590-C-G

72082233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114850450-G-A

http://identifiers.org/hco/12/GRCh38#72082237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114850447-C-A

72082237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114850447-C-G

72082237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114850447-C-T

72082245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114850439-T-A

72082818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849841-C-T

72082822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849837-G-A

72083225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849435-A-G

72083226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849434-T-A

72083267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849393-C-G

72083267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849393-C-T

72083268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849392-G-A

72083393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849270-C-T

72083594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114849067-G-A

72083730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848931-A-T

72084117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848524-A-T

72084122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848519-T-A

72084225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848416-C-T

72084249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848392-G-A

72084352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848298-T-G

72084419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848260-A-G

72084439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848240-T-C

72084475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114848204-T-A

72085675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114847091-G-A

72085748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114847019-T-C

72085788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114847000-T-C

72086042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114846756-C-T

72086395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114844227-G-A

72086608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114844040-A-G

72086669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843980-T-C

72086725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843928-A-T

72086785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843870-G-A

72086865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843791-G-A

72086890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843761-T-C

http://identifiers.org/hco/12/GRCh38#72086994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843678-C-A

72086994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843678-C-G

http://identifiers.org/hco/12/GRCh38#72087045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843629-A-C

72087045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843629-A-T

72087142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843527-T-C

72087192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843482-T-C

72087209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843449-G-A

http://identifiers.org/hco/12/GRCh38#72087227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843431-C-A

http://identifiers.org/hco/12/GRCh38#72087274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843385-A-C

72087274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114843385-A-G

http://identifiers.org/hco/12/GRCh38#72087295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843364-C-A

72087295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114843364-C-T

http://identifiers.org/hco/12/GRCh38#72087311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114843348-C-A

72087311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114843348-C-T

72087342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114843317-G-C

72087342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114843317-G-T

72087525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843134-A-G

72087549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843113-G-A

72087549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114843113-G-T

72088042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842630-A-T

72088047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114842628-G-C

72088186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841285-T-C

72088195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841276-A-G

72088205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841266-T-A

72088291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841186-G-A

72088304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841173-C-G

72088369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841100-T-C

72088393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841077-A-G

72088417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841054-G-T

72088435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841036-G-A

72088438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114841033-A-G

72089875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114840654-G-T

72090100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114840432-C-T

72090185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114840349-G-A

http://identifiers.org/hco/12/GRCh38#72090369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114840164-C-A

72090369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114840164-C-T

72090434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114840099-A-T

72090683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839840-T-A

72090683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839840-T-C

72090736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114839787-T-C

72092456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114836914-C-T

72092597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114836786-A-G

72092626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114836757-A-G

72092656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114836724-G-C

72092665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114836715-G-A

72095069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114831440-C-G

72095069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114831440-C-T

72095089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114831422-T-A

72095213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114831312-T-C

72095673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830784-T-C

72095681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830776-G-A

72095855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830618-T-C

72095951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830524-A-T

72096005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830473-T-C

72096099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830382-G-A

72096099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830382-G-C

http://identifiers.org/hco/12/GRCh38#72096136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114830334-C-A

72096354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114830116-T-C

72096614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114826965-C-T

http://identifiers.org/hco/12/GRCh38#72099286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114824002-A-C

http://identifiers.org/hco/12/GRCh38#72099853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114826066-A-C

72099888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114826029-A-G

72100614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114824392-T-C

72100688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114824322-A-G

72100699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114824311-C-G

http://identifiers.org/hco/12/GRCh38#72100757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114824260-C-A

72101009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114824024-G-A

72101050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114823983-G-A

72101098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114823935-G-A

72101098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114823935-G-C

72101105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114823928-C-T

72101109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114823924-G-A

http://identifiers.org/hco/12/GRCh38#72101687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114823343-A-C

72102162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114822861-G-A

72102558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114822472-T-C

72102609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114822443-A-G

72102667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114822384-G-A

http://identifiers.org/hco/12/GRCh38#72102731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114821991-C-A

72102745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114821977-A-G

72103790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820356-G-C

72103848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820305-T-A

72103927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820228-C-G

72103984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820164-T-A

72104036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820111-G-T

72104136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114820015-G-C

72104158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114819993-A-T

72104234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114819918-C-T

72104246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114819906-C-T

72104486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114819667-C-T

72105004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114819160-A-G

72105146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114818704-G-C

72105560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114818302-G-T

72106547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114816218-T-G

72106709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114815937-A-G

72107486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114814763-G-A

72108294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114812949-T-C

72108583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114812628-G-C

72108769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114812442-T-C

72108924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114812288-T-C

72109089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114812119-T-C

72110801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114806265-C-T

72111002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805947-G-A

72111002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805947-G-T

72111034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805915-C-G

72111054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805895-G-A

72111124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805828-G-A

72111157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805794-G-C

72111230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805725-T-C

72111453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805493-G-T

72111543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805404-C-T

72111802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805149-G-A

72111803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805148-G-A

72111803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114805148-G-T

http://identifiers.org/hco/12/GRCh38#72112001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114804992-A-C

72112208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114804785-C-T

72112558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114804440-C-T

72112584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114804417-T-C

72112620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114804370-T-C

http://identifiers.org/hco/12/GRCh38#72112695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114804295-C-A

72113955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114802011-C-T

72124644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114799376-T-C

72124679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114799266-A-G

72124725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114799223-A-G

72124912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798971-A-G

72124913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798970-T-C

72125169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798729-C-G

72125196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798707-C-G

72125273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798606-C-T

72125298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798581-A-G

72125310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798569-T-C

72125491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798388-T-C

http://identifiers.org/hco/12/GRCh38#72125550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114798336-C-A

http://identifiers.org/hco/12/GRCh38#72125600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114798285-A-C

72125674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798058-G-T

72125687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114798045-G-A

72125908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114797860-A-T

72125931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114797837-C-T

72128127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114797664-C-T

72128163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114797628-T-C

72128399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114797460-T-C

72128870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796985-G-C

72128995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796867-A-G

72129049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796813-C-T

72129381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796506-G-T

72129403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796483-C-G

72129442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796443-C-T

72129487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796393-T-A

72129556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114796333-A-G

72130439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795763-G-T

72130547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795667-T-C

http://identifiers.org/hco/12/GRCh38#72130607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114795598-A-C

72130607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795598-A-G

72130739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795461-G-A

72130746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795453-G-T

http://identifiers.org/hco/12/GRCh38#72130752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114795447-A-C

http://identifiers.org/hco/12/GRCh38#72130849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114795357-A-C

72130849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795357-A-G

72130849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795357-A-T

72130923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114795282-G-A

72131414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114794715-T-A

72131605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114794495-C-T

72131712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114794401-A-G

72132245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114793964-T-G

72132355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114793855-G-A

72132663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114793544-G-A

72132684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114793526-T-C

72133511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114792339-T-A

72133511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114792339-T-G

72133666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114792180-C-T

72133821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791750-C-G

72134080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791489-G-A

http://identifiers.org/hco/12/GRCh38#72134157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114791418-C-A

72134281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791293-A-G

72134347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791227-G-A

72134347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791227-G-T

72134354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114791213-G-A

http://identifiers.org/hco/12/GRCh38#72134502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114790937-C-A

72134711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790732-G-A

72134711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790732-G-T

http://identifiers.org/hco/12/GRCh38#72134728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114790715-C-A

72135061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790234-G-A

72135084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790211-G-A

72135084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790211-G-T

72135085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790210-C-T

72135086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114790209-A-G

72135460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789843-A-G

72135983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789327-G-A

72136134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789185-T-C

72136182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789137-A-G

72136224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789093-C-T

72136248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114789069-A-G

72136615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114788706-T-G

72136636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114788685-A-G

http://identifiers.org/hco/12/GRCh38#72137409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114787121-C-A

http://identifiers.org/hco/12/GRCh38#72137730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114786825-C-A

72137730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114786825-C-T

http://identifiers.org/hco/12/GRCh38#72138705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114786271-C-A

72139391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114785557-C-T

72139541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114785403-G-A

72140765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114785081-T-C

72140989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114784850-T-G

72140992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114784847-T-G

72141078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114784759-A-G

http://identifiers.org/hco/12/GRCh38#72141124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114784713-C-A

72141124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114784713-C-T

72141267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114783251-A-G

http://identifiers.org/hco/12/GRCh38#72141371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114783115-C-A

72141371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114783115-C-T

72141594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114782876-C-T

72143314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114782668-T-C

72143354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114782628-T-C

72143615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114782387-A-G

72144011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114781837-G-A

http://identifiers.org/hco/12/GRCh38#72144095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114780445-A-C

72144466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114780084-G-T

72144626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114779914-T-C

72144658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114779886-A-G

72144951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114779601-G-A

http://identifiers.org/hco/12/GRCh38#72145583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114778975-C-A

72145660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778895-A-G

72145706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778840-G-A

72145800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778725-C-G

72147405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778466-C-T

72147441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778430-A-T

72147534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778340-T-A

72147680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778204-G-T

72147681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778203-A-T

72147727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778161-T-C

72147792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778103-G-A

72147828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778065-G-A

72147828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114778065-G-T

72147850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114778043-G-T

http://identifiers.org/hco/12/GRCh38#72147861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114778031-A-C

http://identifiers.org/hco/12/GRCh38#72147894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114777989-C-A

http://identifiers.org/hco/12/GRCh38#72147927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114777966-C-A

72148039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777866-G-T

72148108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777792-A-G

72148239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777660-A-T

72148452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777441-C-G

72148464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777422-T-C

http://identifiers.org/hco/12/GRCh38#72148593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114777295-A-C

72148615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777273-C-G

72148697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114777181-C-T

72148867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776994-A-G

72148943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776920-T-G

72148974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776889-G-A

72148991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776872-C-T

72149110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776764-C-T

72149171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776701-G-A

72149171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776701-G-C

72149208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776665-T-G

72149278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776602-G-T

72149279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776601-G-A

72149279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776601-G-T

72149342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776546-T-A

72149342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776546-T-C

72149605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776299-G-A

72149605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776299-G-T

72149713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114776185-A-G

72156578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114775246-T-C

72156654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114775174-G-C

http://identifiers.org/hco/12/GRCh38#72158680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114768578-C-A

http://identifiers.org/hco/12/GRCh38#72158681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114768577-C-A

72158681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768577-C-G

72158784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768478-A-T

72158990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768255-A-G

72158992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768253-A-G

72159177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768085-A-T

72159190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114768077-T-C

72159270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114767980-A-T

72160797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114766350-T-C

72160846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114766327-C-G

http://identifiers.org/hco/12/GRCh38#72162073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114765204-A-C

72162440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764864-A-G

72162520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764784-A-G

72162624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764685-A-G

72162852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764423-T-A

72162873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764405-G-A

72162873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764405-G-T

72163063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114764226-G-T

72163137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114764169-G-A

http://identifiers.org/hco/12/GRCh38#72163182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114764122-C-A

72163182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114764122-C-T

http://identifiers.org/hco/12/GRCh38#72163272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114764028-C-A

http://identifiers.org/hco/12/GRCh38#72163302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114764003-C-A

72163378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114763954-T-C

72165546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114762901-T-C

72166971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114762322-G-A

72166971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114762322-G-C

72167008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114762279-G-A

72167273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114762017-C-T

72167356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114761942-G-T

72167641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114761659-A-G

72168162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114761089-G-A

72168194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114761063-G-A

72168222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114761044-A-T

72168334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760889-T-G

72168368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760862-C-T

72168472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760782-G-A

72168780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760469-G-A

72169158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760102-G-A

72169158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114760102-G-T

72169434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759836-C-T

http://identifiers.org/hco/12/GRCh38#72169477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114759795-C-A

72169915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759526-C-T

72170025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759445-G-T

72170092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759384-G-A

72170171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759315-A-T

72170172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759314-A-G

72170230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759256-A-G

72170468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114759034-T-C

72170573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114758931-G-A

72170731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114758822-A-G

http://identifiers.org/hco/12/GRCh38#72170789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114758759-C-A

72170824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114758723-C-G

72170924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114758627-T-C

72171949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114757680-T-G

72172041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114757593-T-C

http://identifiers.org/hco/12/GRCh38#72172056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114757578-A-C

72172524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114756167-T-C

72172809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755913-G-C

72172809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755913-G-T

72172946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755778-C-T

72172986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755738-T-C

72173119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755490-T-G

72173135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755474-T-C

http://identifiers.org/hco/12/GRCh38#72173316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114755290-C-A

72173393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755217-G-T

72173531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755102-G-C

72173534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114755098-C-G

http://identifiers.org/hco/12/GRCh38#72173628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114755000-A-C

72174715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114754112-T-G

72174729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114754098-T-A

72175027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753857-C-G

72175192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753694-T-G

72175201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753685-A-G

72175686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753263-T-C

72175866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753097-T-A

72175893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753068-G-C

http://identifiers.org/hco/12/GRCh38#72175906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114753055-C-A

72175950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114753011-T-G

72176573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114752626-T-C

72176883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114752253-A-T

72177518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751626-A-G

72177579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751576-A-G

72178095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751026-C-G

72178095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751026-C-T

72178787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114750354-G-A

72179006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114750137-T-C

72179528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114749777-A-T

72179667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114749695-C-G

72179729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114749639-A-G

http://identifiers.org/hco/12/GRCh38#72180133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114749268-C-A

http://identifiers.org/hco/12/GRCh38#72180187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114749212-A-C

72180283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114749117-G-A

72180496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748897-T-C

72180529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748861-G-C

72180611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748782-T-A

72180730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748657-A-G

http://identifiers.org/hco/12/GRCh38#72180947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114748461-A-C

http://identifiers.org/hco/12/GRCh38#72181053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#114748356-A-C

72181053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20692
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748356-A-G