7881574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684295-C-T

7881756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684443-T-C

7882001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684654-A-G

7882061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684709-G-T

7882067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684715-T-C

7882115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684767-G-A

7882115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684767-G-T

7882140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684793-G-T

7882347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684935-T-C

http://identifiers.org/hco/6/GRCh38#7882369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38684957-C-A

7882426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38684971-T-G

7882740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685206-G-T

7882830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685286-T-C

http://identifiers.org/hco/6/GRCh38#7882840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38685296-C-A

7882840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685296-C-G

7882840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685296-C-T

7882872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685329-T-C

7882872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685329-T-G

http://identifiers.org/hco/6/GRCh38#7882930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38685391-C-A

7882930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685391-C-T

7883051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685490-G-C

7883051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685490-G-T

http://identifiers.org/hco/6/GRCh38#7883089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38685525-C-A

7883089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38685525-C-T

7884389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38687437-A-G

7884545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687580-C-T

7884578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687587-G-A

7884578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687587-G-C

7884578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687587-G-T

7884579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687588-T-A

7884581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687589-T-C

7884584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687592-G-C

7884584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687592-G-T

7884587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687595-A-G

http://identifiers.org/hco/6/GRCh38#7884645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38687633-A-C

http://identifiers.org/hco/6/GRCh38#7884837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38687790-C-A

7884837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38687790-C-T

7885236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688217-A-G

7885463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688421-C-G

7885737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688541-T-G

7885760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688554-C-T

7885804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688580-G-A

7885859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688630-A-G

http://identifiers.org/hco/6/GRCh38#7885955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38688694-A-C

7885963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 38688702-T-C

7886091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688826-A-G

7886186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688866-A-G

7886244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38688908-G-C

7886776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38689350-T-C

7886892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38689433-G-A

7887063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38689580-T-G

7887275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38689732-G-A

7887922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38690332-C-T

7887994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38690404-C-T

7888165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38690547-C-T

7888176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38690558-T-G

http://identifiers.org/hco/6/GRCh38#7888326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38690649-A-C

7888516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38690809-G-A

7888747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38690967-G-A

7888863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691080-G-A

7888973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691162-T-C

7888973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691162-T-G

7889031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691202-G-T

7889051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691222-T-A

7889051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691222-T-C

http://identifiers.org/hco/6/GRCh38#7889096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38691267-C-A

7889096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691267-C-T

http://identifiers.org/hco/6/GRCh38#7889101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38691272-C-A

7889101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691272-C-T

7889112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691283-T-A

7889112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691283-T-C

7889112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691283-T-G

7889198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691368-A-G

7889222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691392-T-A

7889222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691392-T-C

7889222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691392-T-G

7889225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691395-T-A

7889225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691395-T-C

7889225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691395-T-G

7889246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691413-T-C

http://identifiers.org/hco/6/GRCh38#7889286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38691452-C-A

7889286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691452-C-G

7889355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691536-G-A

7889355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691536-G-C

7889355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691536-G-T

7889404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38691582-G-T

http://identifiers.org/hco/6/GRCh38#7889418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38691596-C-A

http://identifiers.org/hco/6/GRCh38#7889455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38691659-A-C

7889455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38691659-A-G

7889498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38691873-T-C

7889545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38691920-T-G

http://identifiers.org/hco/6/GRCh38#7889707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38692073-C-A

7889707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692073-C-T

7889757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692123-A-G

7889774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692141-A-G

7889795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692167-G-C

7889795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692167-G-T

7890221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692772-C-T

7890300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38692840-C-T

7890623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693137-A-G

7890758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693293-T-C

7890910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693441-C-T

7890974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693467-C-G

7891189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693683-T-A

7891211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693705-G-C

7891381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38693868-C-T

http://identifiers.org/hco/6/GRCh38#7891575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38694058-C-A

7891575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694058-C-T

7891773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694255-G-A

7891773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694255-G-C

7891773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694255-G-T

http://identifiers.org/hco/6/GRCh38#7891797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38694276-C-A

http://identifiers.org/hco/6/GRCh38#7891883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38694349-C-A

7891883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694349-C-T

http://identifiers.org/hco/6/GRCh38#7891910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38694380-C-A

7891910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694380-C-G

7892281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694669-C-G

7892281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694669-C-T

7892358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694721-G-A

7892358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38694721-G-T

7893189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38695867-A-G

7893382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696041-G-C

7893526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696210-G-A

7893584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696270-T-A

7893708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696386-T-C

7893749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696418-G-A

7893837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696492-C-G

http://identifiers.org/hco/6/GRCh38#7893861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38696515-C-A

7893901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696554-A-G

7894932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696902-C-T

7894947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696917-G-A

7894989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696964-T-C

7895036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38696999-G-A

7895222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38697159-C-G

7897835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38700440-G-A

7897938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38700539-T-C

7898480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38700748-C-T

7898494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38700759-G-A

7898641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38700925-G-C

http://identifiers.org/hco/6/GRCh38#7898759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38701022-C-A

7898869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38701096-A-G

7899003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38701230-C-T

7899129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38701331-C-G

7899129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38701331-C-T

http://identifiers.org/hco/6/GRCh38#7899231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38701432-A-C

7899552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38702937-G-T

http://identifiers.org/hco/6/GRCh38#7899740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38703118-A-C

7899751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 38703129-T-C

http://identifiers.org/hco/6/GRCh38#7899829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38703215-C-A

7900082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38703422-A-G

7900505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38703786-C-T

7901010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38704197-G-A

7901694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38705552-A-G

7901751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38705602-T-C

7901751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38705602-T-G

7901932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38705764-G-T

7904271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38706986-C-T

7904317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38707039-T-C

7904428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38707155-C-T

7905052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38707692-G-C

7905264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38707915-T-C

7905331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38707974-C-G

7906750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38709351-G-A

7906752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38709353-A-G

7907221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710076-T-C

7907364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710235-G-A

http://identifiers.org/hco/6/GRCh38#7907386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38710256-C-A

7907396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710266-G-A

7907396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710266-G-C

7907536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710377-G-A

7907555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710398-A-T

7908314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710714-T-A

7908339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710740-C-T

7908348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38710749-G-A

7909323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38711374-G-A

7909731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711701-T-A

7909738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711713-G-A

7909738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711713-G-T

7909741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711717-G-A

7909741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711717-G-C

7909741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711717-G-T

http://identifiers.org/hco/6/GRCh38#7909797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38711762-A-C

7909973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711902-G-A

7909973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711902-G-T

7910002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711934-G-A

7910093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711955-G-A

7910093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711955-G-C

7910093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711955-G-T

7910095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711957-G-A

7910095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38711957-G-T

http://identifiers.org/hco/6/GRCh38#7910148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38712009-C-A

7910148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712009-C-G

7910148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712009-C-T

http://identifiers.org/hco/6/GRCh38#7910226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38712071-C-A

7910226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712071-C-T

7910258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712081-A-G

7910280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712093-G-T

7910286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712099-C-G

7910326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38712106-C-G

7910327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38712107-G-C

http://identifiers.org/hco/6/GRCh38#7910493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38712138-C-A

7910493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712138-C-G

7910493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38712138-C-T

http://identifiers.org/hco/6/GRCh38#7910540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#38712190-C-A

7910540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712190-C-G

7910540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712190-C-T

7910558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712208-G-A

7910558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38712208-G-C

7910558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38712208-G-T

7910684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712307-G-A

7910684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712307-G-C

7910684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38712307-G-T

http://identifiers.org/hco/6/GRCh38#7910768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#38712376-C-A

7910768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21073
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 38712376-C-T