95391376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 5 prime UTR variant
orthologous variants: 76420017-A-G

95391433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: missense variant
orthologous variants: 76419956-G-A

http://identifiers.org/hco/5/GRCh38#95391593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419779-A-C

95391593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: 76419779-A-G

http://identifiers.org/hco/5/GRCh38#95391615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419756-C-A

95391615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: 76419756-C-G

95392646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: 76419604-G-A

95392647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: 76419603-G-T

http://identifiers.org/hco/5/GRCh38#95392677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419566-C-A

95392677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: intron variant
orthologous variants: 76419566-C-T

95392832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76419444-G-A

95392832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76419444-G-C

95392832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76419444-G-T

http://identifiers.org/hco/5/GRCh38#95392879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419397-C-A

95392879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76419397-C-T

http://identifiers.org/hco/5/GRCh38#95392926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419350-A-C

95392927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419349-G-C

95392927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419349-G-T

95392960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419316-G-C

95392960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419316-G-T

95393006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419263-A-G

95393008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419261-T-A

95393008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419261-T-C

http://identifiers.org/hco/5/GRCh38#95393020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76419250-C-A

95393020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419250-C-G

95393020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76419250-C-T

95393469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76418891-T-C

95393527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76418839-T-C

95393620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76418786-C-T

95395062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417567-C-T

95395710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417209-G-A

95395785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417137-G-A

95395804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417118-T-A

95395894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417041-A-G

95395920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76417015-A-G

95395969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416966-A-G

95396012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416946-A-T

95396091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416862-A-T

95396182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76416771-G-A

95396267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416740-T-A

95396268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416739-A-T

http://identifiers.org/hco/5/GRCh38#95396319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76416676-C-A

95396319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416676-C-T

http://identifiers.org/hco/5/GRCh38#95396573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76416420-C-A

95396573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76416420-C-T

95396646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76416321-G-T

95396733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76416242-G-A

95396733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76416242-G-T

95396776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76416199-T-A

95396995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76415998-A-G

95397098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76415907-G-A

95397196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76415856-G-T

95397217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76415836-C-T

95397797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76415286-A-G

95397804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76415279-A-G

95399348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76411634-C-T

http://identifiers.org/hco/5/GRCh38#95399490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76411509-A-C

95399497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76411502-T-C

http://identifiers.org/hco/5/GRCh38#95399787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76411267-A-C

95400361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76410631-A-G

95400361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76410631-A-T

95401489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76409703-G-A

95401621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76407328-C-T

95401747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76407202-G-A

95402158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406795-A-T

95402161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406790-C-T

95402205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406745-C-G

http://identifiers.org/hco/5/GRCh38#95402303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76406665-C-A

95402662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406338-C-T

95402808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406158-G-A

95402914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76406042-A-G

95403141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76405831-A-T

95403596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76405317-C-T

95406600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76404323-T-C

95406630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76404293-G-A

95406630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76404293-G-T

95407050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76403283-C-G

95407171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76403140-G-T

http://identifiers.org/hco/5/GRCh38#95407224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76403063-A-C

95407238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76403049-T-A

95407425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402819-T-A

95407425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402819-T-C

95407767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402492-A-G

95407821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402440-T-G

95407847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402417-A-G

95407893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402371-G-A

95407893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402371-G-C

95407893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402371-G-T

95407943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76402323-T-C

95411146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76401515-G-A

95413423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76401409-T-A

95413914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76400048-G-A

95413914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76400048-G-T

95413970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76399998-T-G

95414047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76399921-G-A

95414101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained, synonymous_variant
orthologous variants: 76399867-C-T

http://identifiers.org/hco/5/GRCh38#95414258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76399731-C-A

95414258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76399731-C-T

http://identifiers.org/hco/5/GRCh38#95414261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76399728-C-A

95414261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76399728-C-G

95414506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76399524-T-C

95414813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76399299-C-T

95414894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76399117-G-A

95415143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76398852-A-G

http://identifiers.org/hco/5/GRCh38#95415440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76398526-A-C

95416294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76398065-A-G

95416342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76398017-T-G

95416695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76397585-T-C

95416782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76397511-A-G

http://identifiers.org/hco/5/GRCh38#95417831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76396943-C-A

95417831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76396943-C-T

95417896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76396887-A-G

95417945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76396837-A-G

95419055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76396425-G-T

95420067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394649-T-A

95420067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394649-T-C

95420067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394649-T-G

95420145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394572-T-G

http://identifiers.org/hco/5/GRCh38#95420167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76394559-C-A

95420167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394559-C-T

95420170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394556-G-A

95420232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394491-T-C

http://identifiers.org/hco/5/GRCh38#95420318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76394405-C-A

95420318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76394405-C-T

95420341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76394382-G-A

95420363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76394360-A-G

95420386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 76394337-C-T

95420387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76394336-G-A

95420387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 76394336-G-C

95420689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76394047-C-T

95420836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76393920-A-T

95420965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76393746-T-G

95421043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76393674-T-C

95421171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76393078-G-A

95421197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76393052-C-G

95421417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392822-G-A

95421486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392754-G-A

95421488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392752-A-G

95421490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392750-G-A

95421572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392670-G-A

95421572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392670-G-C

95422173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76392160-G-C

http://identifiers.org/hco/5/GRCh38#95422220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76392116-A-C

95423005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76391047-G-A

95423462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76390535-G-T

95423582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76390428-G-T

95423683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76390333-C-T

95424277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76389704-A-G

95424292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76389688-A-G

95424319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76389659-G-C

http://identifiers.org/hco/5/GRCh38#95424395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76389589-A-C

95427167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76388192-T-C

95427359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76387996-A-G

95427700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76387720-A-G

http://identifiers.org/hco/5/GRCh38#95427802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76387623-C-A

95427802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76387623-C-G

http://identifiers.org/hco/5/GRCh38#95427841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76387590-C-A

95427841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76387590-C-T

95428419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386965-C-T

95428449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386821-A-G

95428556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386557-A-G

95428556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386557-A-T

95428679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 76386434-A-G

http://identifiers.org/hco/5/GRCh38#95428841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76386281-C-A

95428877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386248-A-T

95428960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386165-C-T

95429107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386039-T-C

95429122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76386024-C-G

95436743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76383196-T-C

95436772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76383165-T-A

95436772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76383165-T-C

95436772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76383165-T-G

http://identifiers.org/hco/5/GRCh38#95436781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76383156-C-A

95436923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76383016-T-C

95437045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76382895-A-G

95437767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76382237-T-A

95437872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76382149-T-C

95437996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76382074-T-C

95438029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76382043-C-T

95438132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76381956-T-C

95438201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76381894-T-C

95438237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76381860-A-G

95441734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376794-T-A

95441761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376767-A-G

95441841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376690-G-C

95441875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376654-T-A

95441982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376549-A-G

95442042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376486-A-G

95442045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376483-T-C

95442243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376312-C-T

95442410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76376154-C-T

95442817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76375860-G-T

http://identifiers.org/hco/5/GRCh38#95443005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76375651-A-C

95443112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76370910-T-C

95443112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76370910-T-G

95443463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 76370226-T-G

95444067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76369703-A-G

95444068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76369702-C-T

95444132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76369637-C-T

95444483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76364108-G-C

95444493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76364098-G-T

95444525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76364066-T-C

95444728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363882-A-T

95444866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363776-C-G

95445085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363403-T-C

95445204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363294-T-C

95445207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363291-A-G

95445265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363236-T-C

95445265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363236-T-G

95445284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363218-T-C

95445309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363193-C-G

95445324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76363178-T-C

95445702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362833-T-A

95445731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362809-G-A

95445739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362801-T-C

95445842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362712-T-C

95445861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362699-T-G

95445902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362664-C-T

95446006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 76362559-A-T

http://identifiers.org/hco/5/GRCh38#95446041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76362501-C-A

95446110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 76362449-A-G

95446722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362195-A-G

http://identifiers.org/hco/5/GRCh38#95446776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76362169-C-A

95446808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362137-G-A

95446808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76362137-G-T

http://identifiers.org/hco/5/GRCh38#95446977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76361949-C-A

95446977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76361949-C-G

95447092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76361620-G-C

http://identifiers.org/hco/5/GRCh38#95447097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76361615-A-C

95447161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76361553-G-A

95447194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76361520-C-G

95447206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76361505-C-T

95447965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76360834-A-T

95448254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76360186-T-C

95448326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 76360057-A-G

95448354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 76360029-C-T

95448373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 76360010-G-A

95448533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76359843-T-C

95448544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76359800-G-A

95448544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76359800-G-T

http://identifiers.org/hco/5/GRCh38#95448597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76359734-C-A

95448913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76359439-A-G

95449103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76359267-A-G

95449324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76358811-C-T

95449416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76358699-C-G

95449487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76358637-G-A

95449487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76358637-G-T

95449625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76358512-C-T

http://identifiers.org/hco/5/GRCh38#95449658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76358479-C-A

95450085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 76350322-A-G

http://identifiers.org/hco/5/GRCh38#95450294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76350113-C-A

95450412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 76349992-A-G

http://identifiers.org/hco/5/GRCh38#95450435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#76349962-C-A

95450435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26335
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 76349962-C-T