http://identifiers.org/hco/11/GRCh38#8612056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109048227-C-A

http://identifiers.org/hco/11/GRCh38#8612152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109048322-A-C

8612279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109048435-T-A

8612279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109048435-T-C

8612463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109048598-G-T

8612706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109048820-C-T

http://identifiers.org/hco/11/GRCh38#8612817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109048919-C-A

8612865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109048966-G-T

8613008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049107-G-A

8613008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049107-G-T

8613047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049137-G-A

8613047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049137-G-T

http://identifiers.org/hco/11/GRCh38#8613207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109049275-C-A

8613207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049275-C-G

8613366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049391-G-A

8613374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049399-C-T

8613375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049400-T-C

8613375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049400-T-G

http://identifiers.org/hco/11/GRCh38#8613386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109049411-C-A

8613386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049411-C-G

8613386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049411-C-T

8613473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049486-A-G

8613558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049674-T-C

8613558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049674-T-G

8613746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049847-G-A

8613746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049847-G-T

8613794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049888-A-G

8613812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049905-G-A

8613812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049905-G-T

8613833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049926-G-C

8613872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109049964-G-A

8613997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050075-A-G

8614000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050078-A-G

8614525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050236-A-G

http://identifiers.org/hco/11/GRCh38#8614570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109050253-C-A

8614570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050253-C-T

8614572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050255-A-G

8614572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050255-A-T

8614649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050335-G-A

8614649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050335-G-T

8614733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050413-G-T

8614763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050438-T-A

8614763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050438-T-C

8615287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050595-T-A

8615342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050652-T-G

8615364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050674-C-T

http://identifiers.org/hco/11/GRCh38#8615392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109050701-C-A

8615459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050753-A-G

8615526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3 prime UTR variant
orthologous variants: 109050809-T-A

8615599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109050900-C-T

8615641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051016-T-G

8615680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051055-T-C

8615696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051071-G-A

8615696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051071-G-T

8615711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051086-T-G

8615749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051120-G-A

8615749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051120-G-T

8615755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051126-G-A

8615776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051147-G-T

8615981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051349-G-T

8616210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051570-G-A

8616210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051570-G-T

8616235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051595-T-C

8616263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051622-G-T

8616358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051718-G-T

8616437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051799-G-A

8616437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051799-G-T

8616490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051832-C-T

8616537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051879-G-T

8616597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109051952-T-A

8616686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052045-T-C

http://identifiers.org/hco/11/GRCh38#8616693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109052052-C-A

8616816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052157-G-A

8616816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052157-G-T

8616845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052181-G-T

8616852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052188-A-G

8616852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052188-A-T

8616882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052200-C-T

8617121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052413-A-G

http://identifiers.org/hco/11/GRCh38#8617295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109052556-C-A

8617295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052556-C-T

http://identifiers.org/hco/11/GRCh38#8617307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109052568-C-A

8617307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052568-C-T

http://identifiers.org/hco/11/GRCh38#8617497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109052758-C-A

8617547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052809-G-C

8617547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052809-G-T

8617553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052811-G-C

8617553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052811-G-T

8617563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052821-G-A

8617563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052821-G-T

8617584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052842-C-T

8617689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052933-G-A

8617689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052933-G-C

8617689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109052933-G-T

8618031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109053261-A-G

8618066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109053295-G-A

8618066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109053295-G-C

8618066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109053295-G-T

8618273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109053803-G-C

8618534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054049-A-G

8618634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054132-G-A

8618634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054132-G-T

8618693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054174-G-A

8618693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054174-G-T

8618701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054182-G-A

8618701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054182-G-T

8618822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109054306-G-A

8618822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109054306-G-T

8618887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109054371-G-A

8619000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109054481-C-G

8619184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109054665-T-C

8619318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054781-T-A

8619318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054781-T-C

8619318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054781-T-G

http://identifiers.org/hco/11/GRCh38#8619331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109054794-C-A

8619331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109054794-C-G

http://identifiers.org/hco/11/GRCh38#8619351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109054814-A-C

http://identifiers.org/hco/11/GRCh38#8619373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109054829-C-A

8619461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109054917-G-C

http://identifiers.org/hco/11/GRCh38#8619550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109055006-C-A

8619550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055006-C-G

8619550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055006-C-T

8619561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055017-G-A

8619561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055017-G-C

8619561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055017-G-T

8619593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055046-T-C

8619593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055046-T-G

8619595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055048-T-C

8619595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055048-T-G

8620053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109055272-G-A

8620053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109055272-G-C

8620086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109055305-G-A

8620193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055388-G-A

8620193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055388-G-T

8620316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109055510-A-T

8620347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056154-C-T

http://identifiers.org/hco/11/GRCh38#8620393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109056201-C-A

8620393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056201-C-T

8620586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056392-T-G

8620588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056394-A-G

8620697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056508-T-A

8620872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056615-G-C

http://identifiers.org/hco/11/GRCh38#8620886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109056629-C-A

8620886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056629-C-T

8620892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056635-A-G

8620901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109056644-C-T

8621058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109056781-A-G

8621215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109056935-G-A

8621236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 109056956-C-T

8621345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057065-C-T

8621416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057141-T-G

http://identifiers.org/hco/11/GRCh38#8621514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109057225-C-A

8621514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057225-C-T

8621543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057236-G-A

8621543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057236-G-T

8621563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057255-G-C

8621563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057255-G-T

http://identifiers.org/hco/11/GRCh38#8621697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109057370-C-A

8621697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109057370-C-G

8621697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109057370-C-T

8621705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109057378-C-T

http://identifiers.org/hco/11/GRCh38#8621818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109057491-C-A

8621818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109057491-C-T

8621829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109057502-G-C

8621829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109057502-G-T

8621859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109057531-T-C

8622688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057826-T-A

8622688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057826-T-C

8622784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057920-G-T

8622810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057942-T-A

8622810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109057942-T-C

8622851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109057983-G-A

8622918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058051-G-A

http://identifiers.org/hco/11/GRCh38#8623004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109058124-A-C

8623004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058124-A-G

8623004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058124-A-T

http://identifiers.org/hco/11/GRCh38#8623005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109058125-C-A

8623207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058289-G-A

http://identifiers.org/hco/11/GRCh38#8623337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109058349-A-C

8623387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058394-G-A

8623443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058447-A-G

8623464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109058472-T-C

8624186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059206-A-G

8624199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059220-T-C

8624210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059225-G-T

8624218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059233-G-T

8624235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059250-G-A

8624235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109059250-G-T

8624309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109059319-A-G

8624313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109059323-G-A

8624313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109059323-G-C

http://identifiers.org/hco/11/GRCh38#8624327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109059337-C-A

8624479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059485-G-A

http://identifiers.org/hco/11/GRCh38#8624587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109059589-C-A

8624587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109059589-C-T

8624628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109059624-T-G

8624689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109059683-G-A

8624689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109059683-G-C

8624700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109059687-C-T

8624814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059807-T-A

8624814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059807-T-C

8624815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059808-G-T

http://identifiers.org/hco/11/GRCh38#8624863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109059856-C-A

8624933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059926-G-C

8624959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109059952-G-A

8624961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059954-G-C

8624988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109059981-G-A

8625136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109060129-G-C

8625293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060279-G-A

8625293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060279-G-C

8625293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060279-G-T

8625324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060310-A-G

8625340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060323-A-G

8625362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060331-C-T

8625376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060345-G-A

http://identifiers.org/hco/11/GRCh38#8625383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109060352-C-A

http://identifiers.org/hco/11/GRCh38#8625517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109060500-A-C

8625539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060522-T-C

8625779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060694-G-A

8626095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109060999-G-C

8626175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061090-A-G

8626424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061347-C-T

http://identifiers.org/hco/11/GRCh38#8626545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109061456-C-A

8626703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061590-T-C

8626715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061602-A-G

8626830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061714-A-T

8626918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061795-C-T

8627070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109061993-T-C

8627096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062013-T-G

8627327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062232-T-C

8627408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062335-C-T

8627457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062384-C-G

8627471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062398-G-A

8627682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109062553-A-G

8628900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109063037-T-G

8628961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109063229-T-G

8629009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109063284-T-A

8629037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109063313-G-A

8629270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109063720-C-T

http://identifiers.org/hco/11/GRCh38#8629400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109063891-A-C

8629820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064320-C-G

8629820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064320-C-T

8629833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064327-G-C

8629978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064716-T-A

8629979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064717-G-A

8630010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064747-C-G

8630238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064940-G-A

8630238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109064940-G-T

8630513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109065186-A-G

8630513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109065186-A-T

8630857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109065661-G-A

8630859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109065663-C-T

8630898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109065685-C-G

http://identifiers.org/hco/11/GRCh38#8630911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109065698-C-A

8631917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067060-G-A

8631932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067071-C-G

8631959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067098-G-C

http://identifiers.org/hco/11/GRCh38#8631963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109067102-C-A

8631963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067102-C-T

8632811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067386-G-A

8632812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067387-T-C

8632820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067395-T-C

8632950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067497-T-C

8633042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067576-G-A

8633097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067625-A-G

8633097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067625-A-T

8633555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109067821-G-C

8634165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109068598-A-T

8634545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109068677-T-C

8634596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109068729-C-T

http://identifiers.org/hco/11/GRCh38#8634770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109068925-A-C

8634882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069015-G-C

8634975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069106-C-T

8635093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069207-A-G

8635138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069251-T-G

8635167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069281-C-G

8635576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069869-A-T

8635603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069886-T-C

8635668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109069960-T-C

8635774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070060-A-G

8636503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070365-T-C

8636726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070553-G-A

http://identifiers.org/hco/11/GRCh38#8636731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109070558-A-C

8636761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070596-G-A

8636811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070632-C-T

8636812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070633-T-C

8637950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070822-G-C

8637950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070822-G-T

8638006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109070875-G-T

http://identifiers.org/hco/11/GRCh38#8638094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109070964-C-A

8638144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109071013-G-T

8638437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071271-A-T

8638528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071353-G-A

8638528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071353-G-T

8638530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071355-T-G

8638561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071386-T-C

8638561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071386-T-G

8638890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109071660-T-C

8639084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109072494-T-C

8639534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109073182-A-G

8639586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109073234-G-A

8639750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109073392-T-C

8639813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109073454-A-T

8639830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109073470-T-G

8640004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109074101-T-G

http://identifiers.org/hco/11/GRCh38#8640117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109074203-C-A

8640117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109074203-C-G

http://identifiers.org/hco/11/GRCh38#8640182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109074241-C-A

8640182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109074241-C-T

http://identifiers.org/hco/11/GRCh38#8640371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109074403-A-C

8640455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109074487-G-T

8640461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074493-G-A

8640461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109074493-G-C

http://identifiers.org/hco/11/GRCh38#8640521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109074553-A-C

8640521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074553-A-G

8640521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074553-A-T

8640554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074562-T-A

8640554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074562-T-C

8640554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074562-T-G

8640560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074568-T-A

8640560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074568-T-C

8640560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074568-T-G

http://identifiers.org/hco/11/GRCh38#8640629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109074637-C-A

8640629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074637-C-T

8640794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074802-C-G

8640794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109074802-C-T

8640912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109074920-G-A

8640912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109074920-G-C

8640919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109074927-T-C

8641082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109075090-T-A

8641082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109075090-T-C

8641082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109075090-T-G

8641175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109075186-T-G

8641313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109075266-G-A

8641326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109075276-C-G

8642231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109075646-G-C

8642424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076333-G-A

8642424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076333-G-C

8642560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076462-A-G

8642638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 109076493-T-C

8642685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant, start_lost
orthologous variants: 109076541-T-C

http://identifiers.org/hco/11/GRCh38#8642841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109076677-C-A

8642841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076677-C-T

8642920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076766-T-A

8642920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076766-T-C

8642920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109076766-T-G

8643013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109076849-A-G

8643094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109076930-T-C

http://identifiers.org/hco/11/GRCh38#8643148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109076983-A-C

8643201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077024-G-T

8643240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077063-T-A

8643240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077063-T-C

8643240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077063-T-G

8643253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077076-T-C

http://identifiers.org/hco/11/GRCh38#8643361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109077196-A-C

8643361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077196-A-T

8643454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109077312-C-T

8644118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109078223-T-C

8644273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109078376-G-T

8644274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109078377-G-A

8644274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109078377-G-T

8644290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109078393-T-C

8644398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109078490-T-C

8644442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109078533-G-A

8644843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109079067-A-G

8645228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109079575-T-C

8645659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080056-G-T

8645692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080087-C-T

8645810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109080202-A-G

8645813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109080205-C-T

8645891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109080284-G-A

8645891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109080284-G-C

8645891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109080284-G-T

8645917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080310-A-G

8645925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080318-A-G

8645976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080371-T-C

8646287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080977-C-G

8646287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109080977-C-T

8646329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081020-A-G

8646329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081020-A-T

8646382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081076-T-C

8646701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081315-A-G

http://identifiers.org/hco/11/GRCh38#8646849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109081441-A-C

8646919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081503-T-A

8646919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081503-T-C

8646919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081503-T-G

8646921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081505-A-G

8647433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081812-C-G

8647433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109081812-C-T

8647712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082057-A-G

8647727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082073-T-C

8647778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082124-G-A

http://identifiers.org/hco/11/GRCh38#8647850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109082175-C-A

8647951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082221-A-T

8647956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082225-C-T

8647959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082228-G-A

8648074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109082343-A-G

8648077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109082346-A-G

8648077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109082346-A-T

8648129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082402-T-C

8648130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082403-A-T

http://identifiers.org/hco/11/GRCh38#8648163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109082433-C-A

8648163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082433-C-G

8648163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082433-C-T

8648210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082468-G-A

8648210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082468-G-T

8648315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082576-G-C

8648315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082576-G-T

8648365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082797-A-G

8648405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109082835-G-A

8648562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109082991-C-G

8648610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083031-G-T

8648618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083039-G-A

8648618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083039-G-T

8648625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083046-T-A

8648625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083046-T-C

8648646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083067-G-A

8648646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083067-G-T

8648670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083091-G-T

8648720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083158-T-A

8648720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083158-T-G

8648794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083232-G-C

8648808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083245-C-T

8649624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083689-T-C

8649716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083776-G-A

8649716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109083776-G-T

8649894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109083939-G-T

http://identifiers.org/hco/11/GRCh38#8650018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109084067-C-A

8650018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084067-C-T

8650728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084296-G-A

8650753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084321-C-T

8650852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084405-G-A

8651318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084824-G-A

8651321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109084827-G-A

8651511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085000-T-C

8651548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085024-T-C

8651771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085225-C-T

8651839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109085293-A-G

8652002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085452-G-A

8652002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085452-G-T

http://identifiers.org/hco/11/GRCh38#8652008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109085458-C-A

8652008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109085458-C-G

8652008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109085458-C-T

8652064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085502-G-A

8652313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109085745-T-C

8652363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085796-G-A

8652395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085831-G-A

8652523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109085964-A-G

8652915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109086337-G-A

8652917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109086339-C-T

8653409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109087823-A-G

8653568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109087977-G-A

8653608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088008-C-T

8654077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088315-A-G

8654162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088388-C-T

http://identifiers.org/hco/11/GRCh38#8654200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109088426-C-A

http://identifiers.org/hco/11/GRCh38#8654277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109088497-A-C

8654361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088577-C-T

8654376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088589-G-T

8654399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088612-C-T

http://identifiers.org/hco/11/GRCh38#8654418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109088631-A-C

http://identifiers.org/hco/11/GRCh38#8654433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109088646-C-A

8654433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 109088646-C-T

http://identifiers.org/hco/11/GRCh38#8654461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109088674-C-A

8654461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088674-C-T

8654594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109088773-A-G

8656851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109091266-A-G

8657356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109091750-G-A

8657633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109091996-T-A

8657633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109091996-T-C

8657653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092016-C-T

8657683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092047-G-A

8657683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092047-G-C

http://identifiers.org/hco/11/GRCh38#8657686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109092049-C-A

8657694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092057-G-A

8657814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092166-T-C

8657832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092183-A-G

8657929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092283-A-G

8658409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092772-T-C

8658487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109092852-C-G

8658487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109092852-C-T

8658555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109092920-G-A

8658810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109093181-G-A

http://identifiers.org/hco/11/GRCh38#8658927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109093298-C-A

8659327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109093658-G-A

8659380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109093724-A-T

8659443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109093786-A-T

8659447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109093790-G-A

8659511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109093848-G-A

8659920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094207-C-G

8660032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094323-G-A

8660032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094323-G-T

8660299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094673-C-T

8660346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094715-G-C

8660410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109094778-C-T

8660572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095314-T-C

8660695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095423-G-A

8660695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095423-G-T

http://identifiers.org/hco/11/GRCh38#8660781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109095488-C-A

8660810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095517-T-A

8660932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095603-G-A

8660944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095615-C-T

8660969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109095640-G-A

8661092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096019-G-A

8661205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096104-C-T

8661214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096112-G-A

8661281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096172-A-G

8661523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096417-T-C

8661552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096443-T-C

8661554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096445-G-T

8661676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096565-T-A

8661676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096565-T-C

8661788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096684-C-T

8661835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096729-C-T

8661881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096777-C-T

8661882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109096778-C-G

8662193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109097090-G-A

8662490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109097392-G-A

8662490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109097392-G-C

8664549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109099320-G-A

8664555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109099322-G-C

8664901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109099623-G-C

8664931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109099654-T-C

8665146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109099867-T-C

8665240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109100144-C-T

http://identifiers.org/hco/11/GRCh38#8665262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109100176-A-C

8665262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109100176-A-G

http://identifiers.org/hco/11/GRCh38#8665312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109100227-C-A

8665342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109100258-C-T

8665424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109100339-T-C

8670791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109106175-C-T

http://identifiers.org/hco/11/GRCh38#8671110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109106315-C-A

8671171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109106380-T-C

8671310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109106498-A-G

8671619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109106782-A-T

8671684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106845-A-G

8671684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106845-A-T

8671747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106909-A-G

8671760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106922-T-C

8671760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106922-T-G

8671761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106923-G-A

8671763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109106925-A-G

http://identifiers.org/hco/11/GRCh38#8671786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109106948-C-A

8671831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 109106984-G-A

8671831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109106984-G-C

8671831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109106984-G-T

8671950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109107103-C-T

8671951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109107104-C-G

8671951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109107104-C-T

8672074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109107218-G-A

8672080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109107224-A-G

8672115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107259-A-G

8672148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107295-A-T

8672156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107303-G-A

8672193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107334-C-T

8672198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107339-C-T

8672227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107344-G-T

8672356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109107480-T-C

8672370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 109107494-G-T

http://identifiers.org/hco/11/GRCh38#8672407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109107529-A-C

8672407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107529-A-G

8672425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107547-T-C

8672475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107607-G-A

8672475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107607-G-T

8672535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107668-G-A

8672535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107668-G-T

8672545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107678-G-A

8672873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107926-T-A

http://identifiers.org/hco/11/GRCh38#8672892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109107944-A-C

8672892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109107944-A-G

8673401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109108540-G-A

8673973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109108988-C-T

8677057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112863-G-A

http://identifiers.org/hco/11/GRCh38#8677103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109112908-A-C

8677103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112908-A-T

8677121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109112925-T-G

8677214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113009-G-A

http://identifiers.org/hco/11/GRCh38#8677217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109113012-A-C

http://identifiers.org/hco/11/GRCh38#8677407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109113216-A-C

8677422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113236-T-C

8677451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113265-C-T

8677454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113268-G-C

8677893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113596-A-G

8677903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113606-T-C

8677912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113619-T-C

8678056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109113970-T-C

http://identifiers.org/hco/11/GRCh38#8678121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109114033-A-C

8678779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109115720-T-C

8678947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109115864-G-T

8678987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109115906-C-T

8679001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109115920-G-A

8679099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109116016-T-C

http://identifiers.org/hco/11/GRCh38#8679100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109116017-C-A

http://identifiers.org/hco/11/GRCh38#8679145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109116054-C-A

http://identifiers.org/hco/11/GRCh38#8679155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109116064-C-A

8679168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116080-A-T

8679206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109116116-T-C

8679223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 109116133-A-G

8679288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116195-G-C

8679442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116297-G-A

8679446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116301-T-C

8679447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116302-G-A

8679468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116322-C-G

http://identifiers.org/hco/11/GRCh38#8679534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109116373-C-A

8679558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116399-T-A

8679558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116399-T-C

http://identifiers.org/hco/11/GRCh38#8679662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109116505-C-A

8679662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116505-C-T

8679702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116527-T-C

8679932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116763-C-T

8680022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109116822-G-A

8680090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116901-G-T

8680122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116932-G-A

8680122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109116932-G-T

8681863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109117923-G-A

http://identifiers.org/hco/11/GRCh38#8682614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118247-C-A

8682614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109118247-C-T

http://identifiers.org/hco/11/GRCh38#8682649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118270-C-A

8682649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109118270-C-G

8682649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 109118270-C-T

8682697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, undefined
orthologous variants: 109118314-G-A

8682697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, undefined
orthologous variants: 109118314-G-C

8682700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, undefined
orthologous variants: 109118316-G-A

8682708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, undefined
orthologous variants: 109118324-C-T

8682757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, undefined
orthologous variants: 109118370-T-C

8682759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 109118372-G-A

8682759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 109118372-G-C

8682759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 109118372-G-T

8682823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 109118436-G-C

http://identifiers.org/hco/11/GRCh38#8682850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118460-C-A

8682850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118460-C-T

8682905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118503-A-G

8682914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118517-G-A

8682914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118517-G-C

8682914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118517-G-T

http://identifiers.org/hco/11/GRCh38#8682940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118540-C-A

8682940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118540-C-G

8682940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118540-C-T

http://identifiers.org/hco/11/GRCh38#8682953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118553-C-A

8682953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109118553-C-T

http://identifiers.org/hco/11/GRCh38#8682965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#109118565-C-A

8682965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109118565-C-T

8683159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29005
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109118741-C-T