26667031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110479413-T-C

http://identifiers.org/hco/11/GRCh38#26667309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110479283-C-A

26667456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110479165-G-A

26667456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110479165-G-T

http://identifiers.org/hco/11/GRCh38#26667544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110479085-C-A

26667612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110479024-T-C

26667695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478941-A-G

26667810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478847-T-C

26667942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478716-A-G

26668139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478557-G-A

26668174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478522-A-G

26668174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478522-A-T

http://identifiers.org/hco/11/GRCh38#26668377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110478364-C-A

26668377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478364-C-T

26668391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478351-G-C

http://identifiers.org/hco/11/GRCh38#26668395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110478347-C-A

26668429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478314-A-T

26668465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478299-A-T

26668567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478218-C-T

26668627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478152-T-A

26668699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110478071-T-C

http://identifiers.org/hco/11/GRCh38#26670403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110477512-A-C

26670475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477439-G-A

26670503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477413-G-T

26670549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477369-G-T

26670550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477368-T-C

26670620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477299-T-A

26670701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477221-G-A

26670701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477221-G-T

http://identifiers.org/hco/11/GRCh38#26670702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110477220-C-A

26670702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477220-C-T

26670750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3 prime UTR variant
orthologous variants: 110477172-G-T

26670848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476977-T-C

26670852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476973-A-G

26670868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476954-G-A

26670868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476954-G-C

26670868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476954-G-T

26670882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476948-G-A

26670882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476948-G-C

26670882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476948-G-T

26670903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476927-G-A

26670903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476927-G-C

26670903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476927-G-T

26670912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476920-T-A

26670912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476920-T-C

26671043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476806-G-A

26671043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476806-G-T

26671053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476796-G-C

26671053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110476796-G-T

http://identifiers.org/hco/11/GRCh38#26671088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110476773-A-C

26671130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110476731-T-A

http://identifiers.org/hco/11/GRCh38#26671269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110476589-A-C

26671290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110476569-T-C

http://identifiers.org/hco/11/GRCh38#26673484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110474732-A-C

26673484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110474732-A-G

http://identifiers.org/hco/11/GRCh38#26673571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110474647-C-A

26673675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110474549-T-A

26673790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110474449-T-C

26673896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110474359-T-C

26674182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110474102-T-C

26674246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110474041-C-T

26678690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110472193-A-G

26678696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110472187-A-G

26678795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110472085-C-G

http://identifiers.org/hco/11/GRCh38#26678861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110472008-C-A

26678872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110472000-T-A

26678872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110472000-T-C

26678881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471992-G-A

26678881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471992-G-T

26678889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471984-T-C

26678897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471976-A-G

26678903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471970-T-C

26678903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471970-T-G

26679193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471618-A-G

26680879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471436-G-A

26681381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470887-T-A

26681472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470749-A-G

26681578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470633-C-T

26681625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470588-C-T

26681862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470256-T-C

26681926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470138-G-C

26681926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470138-G-T

26682070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110470006-G-C

26682186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110469894-T-C

26682187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110469893-A-G

26682433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110469666-A-T

26682583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110471172-G-A

26683697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467581-G-A

26683697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467581-G-C

26683697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467581-G-T

26683739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467545-G-A

26683739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467545-G-C

26683739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467545-G-T

26683806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 110467478-A-G

26683856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467429-G-A

26683856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467429-G-T

26683860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467425-G-A

26683860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467425-G-T

http://identifiers.org/hco/11/GRCh38#26683872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110467413-C-A

26683872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467413-C-G

26683879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467406-T-C

http://identifiers.org/hco/11/GRCh38#26683911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110467368-C-A

26683911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110467368-C-T

26684232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110465306-T-C

26684351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110465192-T-C

26684395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110465149-G-C

26684439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110465107-G-A

http://identifiers.org/hco/11/GRCh38#26684560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110463639-C-A

26684569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110463630-C-G

http://identifiers.org/hco/11/GRCh38#26684604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110463589-C-A

26684618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110463575-G-T

26684723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110463470-C-T

26684731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110463462-G-C

26684839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463385-G-A

26686329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463272-A-T

26686351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463250-A-G

26686393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463209-A-T

26686429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463172-G-A

26686429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463172-G-T

26686580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463020-A-G

26686602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110463014-T-C

26686639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462981-G-A

26686639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462981-G-C

26686639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462981-G-T

26686644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462978-T-C

26686652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462970-G-T

26687009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462669-G-A

26687009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462669-G-C

26687009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462669-G-T

26687070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462602-G-A

26687251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110462415-C-T

26687480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110461810-T-C

http://identifiers.org/hco/11/GRCh38#26687503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110461787-C-A

26687503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110461787-C-T

26687538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110461754-T-C

26691566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110456619-T-C

26691566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110456619-T-G

26691591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110456583-T-C

26691591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110456583-T-G

26692285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110454790-G-T

26692303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110454770-C-T

26692388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110454692-T-G

http://identifiers.org/hco/11/GRCh38#26692707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110454360-C-A

26692707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110454360-C-T

26692712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110454355-G-A

26692727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110454340-T-A

26693314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453867-G-A

26693314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453867-G-C

26693432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453767-A-G

26693479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453711-T-C

26693547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453634-G-T

26693617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453566-G-T

26695074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453380-C-T

26695358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453124-G-C

26695410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453069-T-A

26695410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110453069-T-C

http://identifiers.org/hco/11/GRCh38#26696920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110452426-A-C

26697036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110452297-A-G

26697145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110452162-T-C

26697183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110452127-C-T

26697332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110452015-G-T

26697373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451974-T-C

26697373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451974-T-G

26697381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451967-T-A

26697381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451967-T-C

26697566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451800-C-G

26697859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451496-G-T

26697882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451457-G-A

26697882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451457-G-T

26697884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451455-G-T

26697926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451417-T-A

26697926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451417-T-C

26697934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451409-G-T

26697936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110451392-C-T

26698201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450933-G-A

26698201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450933-G-C

26698221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450914-T-A

http://identifiers.org/hco/11/GRCh38#26698264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110450872-A-C

26698264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450872-A-T

26698265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450871-G-T

26698268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450865-A-G

26698288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450845-G-T

http://identifiers.org/hco/11/GRCh38#26698308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110450826-C-A

26698308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450826-C-T

26698419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110450742-G-A

26698491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110450670-C-T

26698568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450601-T-C

26698568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450601-T-G

http://identifiers.org/hco/11/GRCh38#26698853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110450357-A-C

26698862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110450349-A-G

http://identifiers.org/hco/11/GRCh38#26698891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110450321-C-A

26701804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110449755-A-G

26702145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110449276-A-G

http://identifiers.org/hco/11/GRCh38#26702207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110449222-C-A

26702207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110449222-C-T

26702343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110449087-C-T

26702453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448984-T-C

26702583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448889-A-G

26702584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448888-T-C

26702611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448862-T-C

26702677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448792-G-C

26703019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448439-T-G

26703049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448406-C-T

26703306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448128-C-G

26703306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448128-C-T

26703307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448127-G-A

26703307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448127-G-C

26703307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110448127-G-T

http://identifiers.org/hco/11/GRCh38#26703417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447580-C-A

26703417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447580-C-T

http://identifiers.org/hco/11/GRCh38#26703419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447578-C-A

26703419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447578-C-G

http://identifiers.org/hco/11/GRCh38#26703430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447567-A-C

26703430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447567-A-G

26703431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447566-C-T

http://identifiers.org/hco/11/GRCh38#26703449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447539-C-A

26703449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447539-C-T

http://identifiers.org/hco/11/GRCh38#26703450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447538-C-A

26703450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447538-C-G

26703450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447538-C-T

26703477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110447483-A-G

http://identifiers.org/hco/11/GRCh38#26703808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110447156-C-A

26703808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110447156-C-T

26703889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110447075-C-G

26703889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110447075-C-T

26703974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446989-T-C

26704033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446930-G-A

26704033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446930-G-T

26704533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446468-T-C

26704758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446273-G-A

26704775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446256-G-A

http://identifiers.org/hco/11/GRCh38#26704828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110446179-A-C

26704984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110446001-G-A

26705054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445931-C-T

26705115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445890-T-C

26705133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445873-G-C

26705133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445873-G-T

26705265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445731-T-C

26705620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445393-G-T

26705637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110445376-A-G

26707773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110442149-C-T

26708134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441810-G-T

26708161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441780-T-C

26708221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441716-G-T

26708271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441681-G-A

26708347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441608-G-A

26708347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441608-G-C

26708450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441569-G-A

26708663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441406-G-A

26708765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441306-T-C

26709016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110441090-G-T

26709266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110440590-A-G

26709293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110440554-T-C

26709301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110440546-T-G

26709429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110440408-A-G

26710913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110440184-G-A

26710913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110440184-G-T

26711161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110439920-G-A

26711161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110439920-G-T

26711351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110439766-T-A

26712501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436279-T-C

26712508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436272-T-G

http://identifiers.org/hco/11/GRCh38#26712510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110436270-C-A

26712510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436270-C-T

26712515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436265-T-C

26712555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436223-T-C

http://identifiers.org/hco/11/GRCh38#26712558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110436220-C-A

26712558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436220-C-T

http://identifiers.org/hco/11/GRCh38#26712576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110436202-A-C

26712576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436202-A-G

http://identifiers.org/hco/11/GRCh38#26712621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110436152-C-A

26712621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436152-C-T

26712631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436142-G-A

26712631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436142-G-T

26712645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110436128-T-C

26712648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110436125-A-G

http://identifiers.org/hco/11/GRCh38#26712670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110436103-C-A

26712670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110436103-C-T

26712733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436044-G-A

26712733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436044-G-T

26712746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110436031-A-G

26712778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435616-T-A

26712778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435616-T-C

26712795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435597-G-A

26712795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435597-G-C

26712795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435597-G-T

26712801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435591-T-A

26712801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435591-T-C

http://identifiers.org/hco/11/GRCh38#26712844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110435545-C-A

26712844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435545-C-T

26712856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435533-A-T

26712986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435405-T-A

26713181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110435212-C-T

26716395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110433099-A-G

26716409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110433085-A-T

26716511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432980-T-G

26716516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432974-T-G

26717018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432474-T-C

26717150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432355-A-G

26717245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432273-C-T

26717251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432267-A-G

26717313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110432223-G-C

http://identifiers.org/hco/11/GRCh38#26717617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110431898-A-C

26719164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110429936-A-G

26720568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110429146-A-T

26720658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110429056-T-C

http://identifiers.org/hco/11/GRCh38#26720838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110428874-C-A

26720891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110428824-C-T

26721069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110428645-T-C

26721333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110428364-G-A

26721398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 110428261-G-C

26721723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427936-G-T

26721879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427795-G-A

26721879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427795-G-T

26721904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427773-T-C

26721904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427773-T-G

26721964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427724-G-A

26721964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427724-G-T

26721998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427690-A-G

26722004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427684-T-A

26722014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110427679-A-G

http://identifiers.org/hco/11/GRCh38#26722106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#110427598-A-C

26722106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427598-A-G

26722106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427598-A-T

26722150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427554-T-G

26722439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427289-G-A

26722439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427289-G-C

26722455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110427273-C-G

26722880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110426628-A-G

26722912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110426597-C-T

26722981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28750
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110426533-C-T