25195731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591015-G-A

25195731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591015-G-T

25195832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150591121-T-A

25195832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150591121-T-C

25195832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150591121-T-G

25195860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591146-G-A

25195860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591146-G-C

25195860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591146-G-T

http://identifiers.org/hco/20/GRCh38#25195864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591150-C-A

25195864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150591150-C-T

http://identifiers.org/hco/20/GRCh38#25195865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, start_lost
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591151-A-C

25195865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, start_lost
orthologous variants: 150591151-A-G

25195942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591237-G-A

http://identifiers.org/hco/20/GRCh38#25195950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591282-C-A

25195950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591282-C-G

25195967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591299-G-A

25195967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591299-G-C

25195967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591299-G-T

25195998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150591331-G-A

25196159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150591472-T-C

http://identifiers.org/hco/20/GRCh38#25196215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591532-C-A

25196215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150591532-C-G

25196215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591532-C-T

25196221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591538-G-A

25196221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591538-G-C

25196221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150591538-G-T

25196253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150591555-A-G

http://identifiers.org/hco/20/GRCh38#25196269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591570-C-A

25196269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591570-C-G

25196269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591570-C-T

25196292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591591-G-A

http://identifiers.org/hco/20/GRCh38#25196324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591606-C-A

25196324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591606-C-T

25196326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591608-A-G

25196354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591636-T-A

25196354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591636-T-G

25196355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591637-G-A

25196355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591637-G-C

25196355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591637-G-T

http://identifiers.org/hco/20/GRCh38#25196356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591638-C-A

25196356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591638-C-T

http://identifiers.org/hco/20/GRCh38#25196390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150591671-C-A

25196390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591671-C-T

25196458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150591706-A-G

25196508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150591730-G-A

25196785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 150592045-A-G

http://identifiers.org/hco/20/GRCh38#25196964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592291-C-A

25197015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592344-G-A

25197015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592344-G-T

http://identifiers.org/hco/20/GRCh38#25197018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592347-C-A

http://identifiers.org/hco/20/GRCh38#25197019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592348-C-A

http://identifiers.org/hco/20/GRCh38#25197029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592367-C-A

25197074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592440-A-G

25197124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 150592497-C-G

http://identifiers.org/hco/20/GRCh38#25197193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592554-A-C

25197214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 150592573-G-A

http://identifiers.org/hco/20/GRCh38#25197273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592603-C-A

25197273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592603-C-T

25197324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592629-T-A

25197324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592629-T-C

http://identifiers.org/hco/20/GRCh38#25197326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592631-C-A

25197326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, undefined
orthologous variants: 150592631-C-T

25197338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, undefined
orthologous variants: 150592643-G-A

25197338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, undefined
orthologous variants: 150592643-G-C

25197338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, undefined
orthologous variants: 150592643-G-T

25197403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592701-G-A

http://identifiers.org/hco/20/GRCh38#25197419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150592722-C-A

25197462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150592765-T-C

25205285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593157-T-C

http://identifiers.org/hco/20/GRCh38#25205352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150593215-C-A

25205352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593215-C-T

25205672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593547-C-T

25205812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593649-G-T

25205857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593678-C-T

25206114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150593929-T-C

25206276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594094-G-C

25206332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594156-C-T

25206377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594226-T-A

25206421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594363-T-C

25206434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594376-A-G

25206489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594430-G-A

25206489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594430-G-C

http://identifiers.org/hco/20/GRCh38#25206562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150594498-C-A

25206562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150594498-C-T

25206582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150594518-A-G

25206582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150594518-A-T

25206598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 150594535-T-C

http://identifiers.org/hco/20/GRCh38#25206711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150594655-C-A

25206711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594655-C-T

http://identifiers.org/hco/20/GRCh38#25206936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150594786-C-A

25206936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594786-C-G

25206936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594786-C-T

25207033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594888-G-A

25207033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150594888-G-T

25207084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 150594938-G-A

25207129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 150594985-G-A

25207129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 150594985-G-C

25207129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 150594985-G-T

25207266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150595122-G-A

25207266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150595122-G-T

25207342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150595198-T-A

25207487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595397-T-A

25207492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595402-T-A

25207492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595402-T-C

http://identifiers.org/hco/20/GRCh38#25207495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150595405-A-C

25207495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595405-A-G

25207495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595405-A-T

25207556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595549-G-A

http://identifiers.org/hco/20/GRCh38#25207579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150595572-C-A

25207603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595597-G-C

25207738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595729-C-T

25208038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150595970-G-A

25208322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150596957-T-C

25208322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150596957-T-G

25208432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597028-G-A

25208471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597061-T-G

25209774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597885-G-A

25209774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597885-G-T

25209794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597905-G-A

http://identifiers.org/hco/20/GRCh38#25209810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150597925-A-C

25209810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597925-A-G

25209811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597926-T-C

25209817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150597932-G-A

25209868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 150597982-C-T

25209892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 150598006-A-G

25209907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 150598021-T-C

25209939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150598053-C-T

25211036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150598967-A-G

http://identifiers.org/hco/20/GRCh38#25211178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150599179-A-C

25211233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150599232-C-T

25211335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150599301-C-T

25213223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150600624-G-A

25213328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 150600728-G-T

25213419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150600819-A-G

25213674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150600871-G-A

25213902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601040-A-G

25213942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601086-C-G

25213996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601124-G-A

25214064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601180-C-T

25214086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601202-G-A

25214172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601324-C-T

25214259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601408-C-T

25214299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601436-G-A

25214337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601469-G-A

http://identifiers.org/hco/20/GRCh38#25214346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150601478-A-C

25214428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601611-C-G

25214435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601618-G-C

http://identifiers.org/hco/20/GRCh38#25214569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150601762-A-C

25214647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601852-G-A

25214647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601852-G-T

http://identifiers.org/hco/20/GRCh38#25214655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150601860-C-A

25214655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150601860-C-T

http://identifiers.org/hco/20/GRCh38#25214673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150601871-A-C

25214702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150601875-G-A

25214702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150601875-G-T

http://identifiers.org/hco/20/GRCh38#25214784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150601945-C-A

25214784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 150601945-C-T

25214902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 150602058-A-G

http://identifiers.org/hco/20/GRCh38#25214929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602085-C-A

25214929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: synonymous variant
orthologous variants: 150602085-C-T

25214970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602139-G-A

25214970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602139-G-C

25214970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602139-G-T

25214986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602159-A-G

25214990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602163-G-A

25214992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602165-G-A

25215006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602182-G-A

http://identifiers.org/hco/20/GRCh38#25215010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602186-C-A

25215010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602186-C-T

http://identifiers.org/hco/20/GRCh38#25215021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602197-C-A

25215021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602197-C-G

http://identifiers.org/hco/20/GRCh38#25215056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602234-C-A

25215056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602234-C-G

25215056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602234-C-T

25215115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602279-T-C

25215382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602502-G-A

25215382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602502-G-C

25215475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602687-T-C

http://identifiers.org/hco/20/GRCh38#25215488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602700-A-C

http://identifiers.org/hco/20/GRCh38#25215530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150602758-C-A

25215549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602776-G-C

25215549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602776-G-T

25215554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602781-G-A

25215554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602781-G-T

25215616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150602869-G-A

25215639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150603119-A-G

25215663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron variant
orthologous variants: 150603140-C-T

25215683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: synonymous variant
orthologous variants: 150603160-G-A

25215725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603206-G-A

25215771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603254-T-A

25215771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603254-T-G

http://identifiers.org/hco/20/GRCh38#25215817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150603291-C-A

25215817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603291-C-G

25215817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603291-C-T

http://identifiers.org/hco/20/GRCh38#25215843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150603312-C-A

25215843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603312-C-T

25215860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603350-G-C

25215860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603350-G-T

25216156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603805-T-G

http://identifiers.org/hco/20/GRCh38#25216308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150603925-C-A

25216308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150603925-C-T

http://identifiers.org/hco/20/GRCh38#25216387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604044-C-A

25216387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604044-C-G

25216387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604044-C-T

25216502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604150-G-T

http://identifiers.org/hco/20/GRCh38#25216561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604200-C-A

25216561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604200-C-G

25216561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604200-C-T

25216568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604211-C-T

25216570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604213-T-C

25216572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604215-G-A

25216572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604215-G-T

http://identifiers.org/hco/20/GRCh38#25216617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604259-C-A

25216617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604259-C-T

25216622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604264-T-G

25216623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604265-G-A

25216623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604265-G-T

http://identifiers.org/hco/20/GRCh38#25216645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604293-C-A

25216645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150604293-C-G

25216645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150604293-C-T

http://identifiers.org/hco/20/GRCh38#25216718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604366-C-A

http://identifiers.org/hco/20/GRCh38#25216745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604393-C-A

25216745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604393-C-T

25216749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604397-G-A

25216749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604397-G-T

http://identifiers.org/hco/20/GRCh38#25216779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604417-C-A

25216779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604417-C-T

http://identifiers.org/hco/20/GRCh38#25216780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604418-C-A

25216780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604418-C-T

http://identifiers.org/hco/20/GRCh38#25216787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150604425-C-A

25216794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604432-G-A

25216794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604432-G-T

25216848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604474-G-A

25216848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604474-G-T

25216917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604519-G-C

25217004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604587-C-T

25217109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150604675-C-T

25217448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605436-G-A

25217491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605475-T-G

25217584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605572-C-T

25217600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605580-G-A

25217642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605605-C-T

25217645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605608-G-A

25217645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605608-G-C

25217645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605608-G-T

http://identifiers.org/hco/20/GRCh38#25217663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150605624-C-A

25217676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605637-T-A

25217676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605637-T-C

http://identifiers.org/hco/20/GRCh38#25217703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150605663-C-A

25217703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605663-C-T

http://identifiers.org/hco/20/GRCh38#25217705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150605665-C-A

25218185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150605780-T-A

http://identifiers.org/hco/20/GRCh38#25218580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150606065-C-A

25218635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150606120-G-A

25218635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150606120-G-C

25218635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150606120-G-T

http://identifiers.org/hco/20/GRCh38#25218659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150606131-C-A

25218659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150606131-C-T

25220855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150606967-C-T

http://identifiers.org/hco/20/GRCh38#25220939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150607050-C-A

25220960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607071-C-T

25221019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607131-G-A

http://identifiers.org/hco/20/GRCh38#25221064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150607199-A-C

25221064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607199-A-G

25221204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607342-T-G

25221369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607502-G-A

25221369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607502-G-T

http://identifiers.org/hco/20/GRCh38#25221394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150607524-C-A

25221394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607524-C-T

http://identifiers.org/hco/20/GRCh38#25221455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150607572-C-A

25221455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607572-C-T

http://identifiers.org/hco/20/GRCh38#25221462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150607579-C-A

25221462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607579-C-T

25221531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607653-T-A

25221531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607653-T-C

25221538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607660-G-T

25221547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607669-T-C

25221563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607685-A-G

25221618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607742-G-A

25221618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607742-G-T

25221671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607801-G-A

25221671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607801-G-T

25221688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607823-T-C

25221759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607904-G-T

25221762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150607907-C-G

25221940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608169-G-T

25221999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608221-G-A

25221999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608221-G-T

25222020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608241-A-G

25222083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608292-G-T

25222100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608309-A-G

http://identifiers.org/hco/20/GRCh38#25222113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150608321-C-A

25222113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608321-C-T

25222122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608326-A-G

25222161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608351-T-C

25222165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608357-G-A

25222165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608357-G-C

25222165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608357-G-T

25222188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608377-T-C

25222188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608377-T-G

25222242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608436-T-C

25222242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608436-T-G

http://identifiers.org/hco/20/GRCh38#25222247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150608441-C-A

25222247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608441-C-G

25222287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608474-G-A

25222287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608474-G-T

25222295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608475-G-T

25222328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608506-A-G

25222328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608506-A-T

25222339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608511-T-C

25222339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608511-T-G

25222355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608528-G-A

25222355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608528-G-C

25222355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608528-G-T

25222375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608549-G-A

http://identifiers.org/hco/20/GRCh38#25222476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150608653-C-A

25222476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608653-C-T

25222480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608657-T-C

25222521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608697-G-A

25222521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608697-G-T

25222565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608719-G-A

25222565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608719-G-C

25222565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608719-G-T

25222579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608733-A-G

http://identifiers.org/hco/20/GRCh38#25222775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150608808-C-A

25222784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150608817-G-C

25222784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 150608817-G-T

25222814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150608846-C-T

http://identifiers.org/hco/20/GRCh38#25222993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150609029-A-C

25222993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150609029-A-G

25222993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150609029-A-T

25223024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150609060-G-A

25223024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150609060-G-C

25223024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150609060-G-T

25223206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150609178-C-G

http://identifiers.org/hco/20/GRCh38#25223806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150610374-C-A

25223806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150610374-C-T

25223857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150610427-C-G

25224004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150610694-G-T

25224048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150610739-G-A

25224167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150610851-G-C

25224167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150610851-G-T

http://identifiers.org/hco/20/GRCh38#25224221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150610903-C-A

25224221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150610903-C-T

25225229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150612236-C-T

http://identifiers.org/hco/20/GRCh38#25225407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150612413-C-A

25225573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150612623-C-T

http://identifiers.org/hco/20/GRCh38#25225910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150612957-C-A

25225910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150612957-C-T

25225954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150612990-T-A

25225954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150612990-T-C

25225956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150612992-C-T

http://identifiers.org/hco/20/GRCh38#25225974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613015-C-A

25225974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613015-C-T

http://identifiers.org/hco/20/GRCh38#25225978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613019-C-A

25225978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613019-C-G

25225978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613019-C-T

25226049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613088-G-A

25226049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613088-G-T

25226151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613141-G-T

http://identifiers.org/hco/20/GRCh38#25226170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613159-C-A

25226170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613159-C-G

25226170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613159-C-T

http://identifiers.org/hco/20/GRCh38#25226231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613243-C-A

25226231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613243-C-T

25226252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613264-C-T

http://identifiers.org/hco/20/GRCh38#25226257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613269-C-A

25226304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613299-G-A

25226304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613299-G-T

25226320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613316-T-C

25226483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613443-G-A

25226483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613443-G-C

25226483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613443-G-T

25226537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150613471-C-T

http://identifiers.org/hco/20/GRCh38#25226838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613680-C-A

25226838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613680-C-T

25226839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613681-G-A

25226839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613681-G-T

http://identifiers.org/hco/20/GRCh38#25226871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#150613705-C-A

25226871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613705-C-T

25226876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613711-G-T

25227032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613841-G-A

25227032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150613841-G-T

25227267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 150614509-T-C

25227277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 150614519-C-T

25227300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150614538-C-T

25227365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150614603-C-T

25227862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150615039-C-G

25227862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3368
most severe consequence: 3 prime UTR variant
orthologous variants: 150615039-C-T