34457584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568573-G-A

http://identifiers.org/hco/9/GRCh38#34457593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41568582-C-A

34457593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568582-C-T

34457782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41568765-C-T

http://identifiers.org/hco/9/GRCh38#34458069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41569043-C-A

34458069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569043-C-T

http://identifiers.org/hco/9/GRCh38#34458164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41569137-C-A

34458164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41569137-C-T

http://identifiers.org/hco/9/GRCh38#34458296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41569269-C-A

34458296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41569269-C-G

34458296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41569269-C-T

34458351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569324-G-A

34458351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569324-G-T

http://identifiers.org/hco/9/GRCh38#34458376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41569349-A-C

34458376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569349-A-G

34458416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569382-G-A

34458416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569382-G-T

http://identifiers.org/hco/9/GRCh38#34458519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41569486-C-A

34458605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569572-G-A

34458605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569572-G-T

34458640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569607-G-A

34458640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569607-G-C

34458640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569607-G-T

34458798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569767-G-A

34458798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569767-G-T

34458868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569839-G-A

34458868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41569839-G-T

34459023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 41569988-G-A

34459023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 41569988-G-T

34459775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570358-T-G

34459872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570459-A-G

34460052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570560-C-T

34460337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570761-T-G

34460481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41570935-G-C

34461377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41571193-G-A

34461649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41571442-G-A

34461987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41571734-A-G

34462339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572519-C-G

34462393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572573-T-A

34462441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572621-G-A

34462468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41572648-T-A

34462842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573006-T-C

34462993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573162-T-G

http://identifiers.org/hco/9/GRCh38#34463034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41573202-A-C

34463048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573216-G-A

34463055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573223-C-T

34463175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41573331-T-C

34463714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41573883-G-A

34464612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41574984-C-T

34464629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41575001-C-T

34464649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41575012-A-G

34464708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41575068-T-G

34464723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41575092-T-C

34465129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41575451-G-A

34465784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576126-A-G

34466178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576438-G-A

34466264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576515-T-C

http://identifiers.org/hco/9/GRCh38#34466277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41576528-C-A

34466392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576630-T-G

34466451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576693-T-G

34466526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41576763-G-A

34466597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577175-G-A

34466597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577175-G-T

34466671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577248-A-G

34467069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577654-G-T

34467178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577757-C-T

34467276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41577855-A-G

34467964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41578222-G-T

34472231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41583656-A-G

34472277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41583696-T-C

http://identifiers.org/hco/9/GRCh38#34474966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41587555-A-C

34475507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41588077-A-G

34475641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41588169-C-G

34475902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589560-G-A

34475902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589560-G-C

34475939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589598-G-A

34475975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589634-G-A

34476068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589727-A-G

34476148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589804-G-A

34476148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589804-G-T

34476224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41589871-C-T

34476648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41590564-G-C

34476771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41590686-T-C

34476873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591307-T-C

34476986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591406-C-T

34477307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591474-G-A

34477388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591554-T-C

34477434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591591-G-A

34477533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41591716-G-A

34478639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41591793-G-T

http://identifiers.org/hco/9/GRCh38#34478798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41591941-A-C

34478798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41591941-A-G

34478904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41592066-A-G

34478990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41592176-A-G

34479162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41592346-C-T

34479582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41593770-C-G

34479582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41593770-C-T

http://identifiers.org/hco/9/GRCh38#34479688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41593849-A-C

34479698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41593859-C-G

34479698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41593859-C-T

34483414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596211-A-G

34483542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596337-A-G

34483562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596357-G-T

34483575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596363-A-G

34483825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596567-T-C

34483873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596615-G-A

34484408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41596846-A-T

34484765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597199-T-G

34484845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597283-G-A

http://identifiers.org/hco/9/GRCh38#34484921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41597351-C-A

34484921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597351-C-G

http://identifiers.org/hco/9/GRCh38#34484926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#41597356-C-A

34484926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597356-C-T

34484975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597405-T-A

34484975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597405-T-C

34484978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41597408-G-A

34485054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41597488-C-T

34485066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41597500-G-T

34485261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41597698-T-C

34485289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41597720-G-A

34485324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41597752-T-C

34485552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41597973-C-G

34485668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41598084-T-C

34486201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41599008-G-A

34486275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41599081-A-G

34486778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600030-A-T

http://identifiers.org/hco/9/GRCh38#34487569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41600504-C-A

34487597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600532-C-G

34487759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600676-T-C

http://identifiers.org/hco/9/GRCh38#34487778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41600695-C-A

34487788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600705-A-G

34487814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600728-T-C

34487815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600729-C-T

34487826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600738-A-G

34487843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41600755-T-C

34488093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600844-T-C

34488113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600860-T-C

34488130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600877-A-G

34488130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600877-A-T

34488135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600882-G-A

34488247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600960-G-A

34488247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41600960-G-C

34488288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41601001-A-G

34488459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41601163-T-C

http://identifiers.org/hco/9/GRCh38#34488463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41601167-C-A

34488463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41601167-C-T

34488502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41601215-T-C

34488564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41601282-A-G

http://identifiers.org/hco/9/GRCh38#34488581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41601299-C-A

34488862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41601579-G-A

34488897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41601687-T-C

34488897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41601687-T-G

34489029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41601824-G-T

34489169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41602133-T-C

34489175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41602139-G-A

34489192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41602157-T-C

34489227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602190-A-G

34489233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602271-T-A

34489233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602271-T-C

34489433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41602628-C-T

34489473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602668-G-A

34489473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602668-G-T

34489506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602685-T-C

34489546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602715-G-T

34489885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602753-A-G

http://identifiers.org/hco/9/GRCh38#34489915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41602774-C-A

34489915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602774-C-T

34489957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602811-C-T

http://identifiers.org/hco/9/GRCh38#34489960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41602814-A-C

34489973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602827-A-G

http://identifiers.org/hco/9/GRCh38#34489979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41602833-A-C

34489986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41602840-G-A

34490086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41602961-A-G

34490138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603015-T-A

34490171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603044-G-T

http://identifiers.org/hco/9/GRCh38#34490270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41603120-C-A

34490270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603120-C-T

34490272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603122-T-C

http://identifiers.org/hco/9/GRCh38#34490304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41603150-C-A

34490331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603184-C-T

34490333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603186-C-T

34490452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41603306-T-C

http://identifiers.org/hco/9/GRCh38#34490503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41603352-A-C

34490627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603452-G-T

34490628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603453-G-T

34490853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603600-T-C

34490976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603719-A-G

34491133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603851-T-A

34491163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41603879-C-G

34491265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604000-C-T

34491303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604035-G-T

34491361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41604091-T-C

http://identifiers.org/hco/9/GRCh38#34491407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41604135-C-A

34491407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41604135-C-T

34491588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604316-A-G

34491588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604316-A-T

34491618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604347-G-A

34491618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604347-G-T

34491619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604348-C-G

34491619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604348-C-T

34491643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604374-G-T

http://identifiers.org/hco/9/GRCh38#34491683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41604413-C-A

34491683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41604413-C-T

http://identifiers.org/hco/9/GRCh38#34492114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41604786-A-C

34492424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605073-C-G

34492438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605087-G-A

34492517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605163-T-G

http://identifiers.org/hco/9/GRCh38#34492938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41605445-C-A

34492991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605498-G-T

http://identifiers.org/hco/9/GRCh38#34493091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41605608-C-A

34493091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605608-C-G

34493091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605608-C-T

34493096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605613-G-A

34493096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605613-G-T

34493127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605636-G-T

34493146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605652-G-C

34493155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41605661-G-A

34493343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41605843-C-G

34493344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41605844-C-G

34493344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41605844-C-T

34493388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41605887-G-T

34493452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41605952-G-A

34493546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606041-C-G

34493609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606096-C-T

34493736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606265-T-G

34493879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606737-T-C

34493991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606840-C-T

34493992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41606841-G-A

34494419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41607267-A-G

34494503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41607351-C-T

34494691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41607625-G-A

34494696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41607630-G-A

34494966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41607904-C-T

34495144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608076-T-C

34495259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608167-G-A

34495475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608304-C-T

34495513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608342-G-A

34495733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608503-G-A

34495804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608565-C-G

34496055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41608803-G-C

34496293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609206-C-T

34496309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609222-A-T

34496408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609557-A-G

34496420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609569-C-T

34496615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609732-C-T

http://identifiers.org/hco/9/GRCh38#34496780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41609883-C-A

34496818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609930-G-A

34496880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41609989-G-C

34497000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610102-G-A

34497005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610107-G-T

http://identifiers.org/hco/9/GRCh38#34497037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41610139-C-A

34497037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610139-C-G

34497037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610139-C-T

http://identifiers.org/hco/9/GRCh38#34497260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41610557-C-A

34497260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610557-C-G

34497260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610557-C-T

34497395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610699-T-C

34497476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610776-G-C

34497495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610794-G-A

34497495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610794-G-C

34497506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41610807-A-G

34498022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41611645-T-C

34498113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41611709-G-A

34498158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41611752-A-T

34498185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41611778-A-G

34498250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41611844-A-G

34498531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612121-T-C

34498622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612212-A-G

34499018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612607-C-G

http://identifiers.org/hco/9/GRCh38#34499043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41612632-A-C

34499155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612745-C-T

34499189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612779-C-T

34499246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41612854-T-C

34499502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613104-T-G

34499509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613111-C-T

34499604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613187-G-A

34499749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613292-A-T

34500212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613764-T-C

34500424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613967-T-A

34500437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41613980-A-G

34500514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614040-A-G

34500531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614057-C-T

34500566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614091-T-C

34500709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, undefined
orthologous variants: 41614217-G-A

34500709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron_variant, undefined
orthologous variants: 41614217-G-C

34500815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: missense_variant, undefined
orthologous variants: 41614323-G-A

34500968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614480-G-A

34500968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614480-G-T

http://identifiers.org/hco/9/GRCh38#34501085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41614598-C-A

http://identifiers.org/hco/9/GRCh38#34501093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41614606-C-A

34501093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614606-C-T

34501197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614709-A-G

http://identifiers.org/hco/9/GRCh38#34501252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41614764-C-A

34501256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614768-T-C

34501290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614819-G-A

34501290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614819-G-T

http://identifiers.org/hco/9/GRCh38#34501302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41614831-C-A

34501302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614831-C-T

34501308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41614837-A-G

http://identifiers.org/hco/9/GRCh38#34501328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41615089-C-A

34501745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41615399-C-G

34501839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41615518-C-T

34502858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41616451-G-A

34502957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41616530-G-A

34503165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41616712-C-T

34503376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41616870-C-T

34503777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41617811-T-C

http://identifiers.org/hco/9/GRCh38#34503807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41617841-C-A

34503941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41617974-G-A

34504151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41618186-C-T

34504706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41618717-C-G

34504871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41618878-C-T

34504988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41618973-T-A

34504988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41618973-T-C

34505342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41619312-G-A

34506097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624061-A-G

34506097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624061-A-T

http://identifiers.org/hco/9/GRCh38#34506131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41624099-C-A

34506131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624099-C-G

34506155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624123-C-T

34506362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624790-T-C

34506363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624791-T-C

34506495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41624928-G-T

http://identifiers.org/hco/9/GRCh38#34506512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41624945-C-A

34506691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41625168-T-C

34506691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41625168-T-G

34506882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41625359-A-G

34506882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 41625359-A-T

34506916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41625380-G-A

34507129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41625576-C-T

34508425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41626179-C-T

34508554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41626270-T-C

34509276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41627126-G-T

34509624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41627486-C-G

34509659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41627518-T-C

34510149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41627844-A-G

34510979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41628594-G-C

34512162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41629845-A-G

34512165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41629848-T-C

34512223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41629906-C-T

34512227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41629910-G-A

34512357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 41630017-T-C

34512358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 41630018-G-A

34512785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41630376-G-A

34512825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 41630417-C-T

http://identifiers.org/hco/9/GRCh38#34513078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41630566-C-A

34513279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41630777-T-C

http://identifiers.org/hco/9/GRCh38#34513309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41630819-C-A

34513342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41631184-G-A

34513342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41631184-G-T

34513530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41631348-G-T

34513556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41631385-G-C

34513654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41631484-A-G

34514343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632073-G-A

34514343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632073-G-T

34514388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41632133-G-A

34514388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41632133-G-C

34514388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41632133-G-T

http://identifiers.org/hco/9/GRCh38#34514435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41632181-C-A

34514435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41632181-C-G

34514435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41632181-C-T

34514575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41632324-C-G

34514801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632547-G-A

34514801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632547-G-T

34514867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632615-G-A

34514867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632615-G-T

34515021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632770-G-A

34515113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632823-G-T

34515139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41632849-A-T

34515898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41633611-A-G

34516365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41634275-T-C

34517089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41634816-A-G

34517102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41634829-C-T

34517713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635367-G-A

34517788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635435-G-A

34517828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635474-G-A

34517841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635486-G-A

34517991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635627-A-G

34518011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635647-A-G

34518039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41635676-G-A

34519182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41636611-G-A

34519205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41636634-T-C

34519299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41636710-A-G

34519507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41636912-A-G

34519775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637136-G-A

34519817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637154-G-A

34519831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637168-G-C

34519934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637269-T-C

34520077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637409-C-T

34520380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637632-A-T

34520476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637726-T-C

34520491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637741-G-A

34520491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637741-G-C

34520491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637741-G-T

34520527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637751-A-G

34520529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637753-G-A

34520529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: 41637753-G-T

http://identifiers.org/hco/9/GRCh38#34520584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41637798-A-C

34520696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: synonymous_variant, undefined
orthologous variants: 41637911-G-A

34520696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: synonymous_variant, undefined
orthologous variants: 41637911-G-T

34520702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: synonymous_variant, undefined
orthologous variants: 41637917-T-A

34520846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 41638023-G-A

34520846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 41638023-G-T

34520974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 3 prime UTR variant
orthologous variants: 41638141-G-A

34520974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2954
most severe consequence: 3 prime UTR variant
orthologous variants: 41638141-G-T