92702944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935689-G-T

92702975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935660-G-T

92702999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 95935637-G-T

92703039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935600-C-T

92703053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935586-C-G

92703057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935582-C-T

92703113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5 prime UTR variant
orthologous variants: 95935513-A-G

92703170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95935463-C-G

92703170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95935463-C-T

92703251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron_variant, undefined
orthologous variants: 95935378-T-C

92703550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95934935-G-A

92703732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95934757-C-T

92703843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95934621-C-G

92704307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95934012-C-T

92704312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95934007-C-G

92704382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95933912-T-C

92704459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95933818-C-T

92704701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95933603-C-T

92704964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95933504-C-G

92705071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95933397-T-G

92705586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95932924-C-T

92705627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95932884-G-T

92705697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95932812-C-T

http://identifiers.org/hco/12/GRCh38#92705935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95932591-C-A

92706136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95932341-T-A

92706347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: intron variant
orthologous variants: 95932125-A-G

92706489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95932004-C-T

http://identifiers.org/hco/12/GRCh38#92706515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95931977-C-A

92706515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95931977-C-G

92706521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95931971-G-A

92706570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95931928-C-T

92706582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 95931916-A-G

92706664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: synonymous variant
orthologous variants: 95931826-G-T

92706666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: 95931824-C-G

92706666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: 95931824-C-T

92706700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: synonymous variant
orthologous variants: 95931802-G-A

92706801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: 95931701-G-A

92706827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: 95931657-T-C

92706901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 95931583-A-G

92706991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 95931493-C-T

http://identifiers.org/hco/12/GRCh38#92707013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95931471-C-A

92707013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 95931471-C-G

92707020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: 95931464-A-T

92707022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: stop_gained, synonymous_variant
orthologous variants: 95931462-A-T

http://identifiers.org/hco/12/GRCh38#92707044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95931440-A-C

92707118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 95931383-C-G

92707118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: synonymous variant
orthologous variants: 95931383-C-T

92707246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931283-A-G

92707327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931208-A-G

92707368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931160-G-A

92707369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931159-G-A

92707369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931159-G-T

92707420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931125-T-G

92707446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931094-G-T

92707448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931092-A-G

92707455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 95931085-C-T

92707697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 95930830-G-C

92707705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 95930822-A-G

92707818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930715-A-G

http://identifiers.org/hco/12/GRCh38#92707835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95930698-C-A

92707835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930698-C-T

92707906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930599-T-A

92708048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930456-A-G

92708120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930281-G-T

92708124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930277-T-C

92708243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930176-T-A

92708243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930176-T-C

92708269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930150-G-T

92708348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 95930096-G-T

92708568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929934-T-C

http://identifiers.org/hco/12/GRCh38#92708652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95929846-A-C

92708693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95929833-G-A

92716525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95928215-T-G

92716685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95928081-G-A

92716867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95927986-T-C

92717139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95927716-A-G

92717174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95927680-T-C

92717334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95927548-T-A

92717978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926878-G-A

92717991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926865-T-A

92722261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926711-G-A

92722320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926656-T-C

92722364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926610-T-C

92722402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926572-C-G

92722402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926572-C-T

92722592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926386-C-T

92722628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926351-T-C

92722727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926287-T-C

92722729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926285-G-C

92722761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926192-G-C

92722944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95926006-A-G

92722956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925994-G-A

92722978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925958-T-A

92723041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925899-T-C

92723243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925775-G-C

92723320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925695-A-G

92725331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925284-T-C

92726866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95925194-G-T

92727225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95924893-C-T

92727227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95924891-G-A

http://identifiers.org/hco/12/GRCh38#92728982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95924855-C-A

http://identifiers.org/hco/12/GRCh38#92728988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95924849-C-A

92729014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95924823-T-C

92729014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95924823-T-G

92729093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95924730-T-C

92729098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95924725-T-C

http://identifiers.org/hco/12/GRCh38#92729231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95924595-C-A

http://identifiers.org/hco/12/GRCh38#92729318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95924515-C-A

92729318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95924515-C-T

92729478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95924337-C-T

92731996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95922195-A-T

http://identifiers.org/hco/12/GRCh38#92732095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95922107-C-A

http://identifiers.org/hco/12/GRCh38#92732144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95922058-C-A

http://identifiers.org/hco/12/GRCh38#92732151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95922051-C-A

http://identifiers.org/hco/12/GRCh38#92732167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95922035-C-A

http://identifiers.org/hco/12/GRCh38#92732388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95921817-A-C

92732415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921788-T-C

92732595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921600-T-A

92732750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921456-T-A

92732796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921410-G-C

92732832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921369-G-A

92732904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95921307-G-A

92733128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920808-A-G

92733191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920745-G-T

92733607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920242-T-G

92733848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95920017-G-A

92733887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919986-A-G

92733934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919953-C-G

92734039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919340-G-A

92734090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919289-C-T

http://identifiers.org/hco/12/GRCh38#92734391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95919077-C-A

92734448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95919019-T-C

92734768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918964-G-C

http://identifiers.org/hco/12/GRCh38#92734844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95918900-A-C

92734984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918777-A-G

92735016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918745-C-T

92735038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918723-A-G

92735089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918676-G-A

92735102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918663-C-T

http://identifiers.org/hco/12/GRCh38#92735232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#95918551-A-C

92735656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918172-G-C

92735671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 95918157-C-T

92735858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95918011-T-G

92735939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917485-T-C

92735960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917464-T-A

92735975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917433-A-T

92735987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95917421-G-A

92736235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95916837-A-T

92736294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95916778-A-G

92736350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95916722-G-A

92736385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95916678-G-A

92736385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95916678-G-T

92736494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95916565-C-G

92736509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95916545-G-A

92736509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95916545-G-T

92736927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95915764-C-T

92736963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95915731-G-A

92737052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95915650-A-G

http://identifiers.org/hco/12/GRCh38#92737229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95915422-C-A

92737229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95915422-C-T

92737382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95915300-A-T

http://identifiers.org/hco/12/GRCh38#92737476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95915230-A-C

92737477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95915229-A-G

92737483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95915223-T-C

92740157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95912301-T-C

92740237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95912255-A-G

92740578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911957-G-A

92740702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911838-T-C

92740724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911824-T-G

http://identifiers.org/hco/12/GRCh38#92740733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95911815-C-A

92740733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911815-C-T

92740743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911805-C-T

92740776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911772-T-A

92740837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911712-A-G

http://identifiers.org/hco/12/GRCh38#92740880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95911668-C-A

92740880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95911668-C-G

92742221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911274-A-G

92742357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95911151-T-G

92742972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910756-T-C

http://identifiers.org/hco/12/GRCh38#92742981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95910747-C-A

92742982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910746-C-T

92743314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910512-C-T

92743379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910452-T-C

92743459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910366-T-C

92743507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95910318-G-T

92750236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95902902-T-C

92750322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95902812-A-G

92750323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95902811-G-A

http://identifiers.org/hco/12/GRCh38#92750338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95902796-A-C

92750371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95902765-T-C

92750537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95902594-C-G

92753591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95901278-G-A

92753664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95901212-C-T

http://identifiers.org/hco/12/GRCh38#92753886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95901026-C-A

http://identifiers.org/hco/12/GRCh38#92753976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95900941-A-C

92754022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900887-A-T

92754032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900863-C-G

92754117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 95900765-C-T

92754149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 95900708-A-G

92754204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95900584-A-G

http://identifiers.org/hco/12/GRCh38#92754261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#95900442-A-C

92754261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 95900442-A-G

http://identifiers.org/hco/12/GRCh38#92754317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#95900384-C-A

92754317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 95900384-C-T

92754321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 95900380-A-G

92754352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900350-T-C

92754352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900350-T-G

92754393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900319-A-G

92754562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95900160-G-A

92755001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95899769-T-G

92755032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95899739-T-C

92755197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95899610-G-A

92755674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95898980-G-T

http://identifiers.org/hco/12/GRCh38#92755729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95898925-C-A

92755729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95898925-C-T

92755778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95898876-A-G

92755779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95898875-A-G

http://identifiers.org/hco/12/GRCh38#92755789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95898865-C-A

92755789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95898865-C-T

92755808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95895233-T-C

92755845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95895196-A-G

92755877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 95895164-T-A

92755896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95895145-T-A

http://identifiers.org/hco/12/GRCh38#92755935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95895106-C-A

92755935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95895106-C-T

92756092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894957-T-C

92756092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894957-T-G

92756213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894831-A-T

92756231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894813-G-A

92756231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894813-G-C

92757009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894057-A-G

92757082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95894011-T-C

92757108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95893989-C-G

92757263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95893848-C-T

92757595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95893521-A-G

92760784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95891110-T-C

92761356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95889662-A-G

92761489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95889554-G-T

92761819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95889370-G-A

http://identifiers.org/hco/12/GRCh38#92761948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95889275-C-A

92761948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95889275-C-T

92762061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95889207-G-A

92762301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95888951-C-T

92763510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95888332-C-G

92764045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95888146-T-C

92764162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95888057-T-C

http://identifiers.org/hco/12/GRCh38#92764182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95888037-C-A

92764182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95888037-C-T

92764224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95887997-T-G

92768706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885714-A-G

92768782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885663-T-C

92768921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885560-G-T

92769198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885347-G-A

92769198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885347-G-C

92769439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885175-T-C

http://identifiers.org/hco/12/GRCh38#92769484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95885131-A-C

92769589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95885005-C-G

http://identifiers.org/hco/12/GRCh38#92769643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95884950-A-C

92769711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95883886-T-C

92769789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95883813-T-C

92770029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95883638-G-A

92770029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95883638-G-C

92770158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95883525-C-G

92770158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95883525-C-T

92770195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_lost
orthologous variants: 95883488-G-T

92770238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883450-T-A

92770238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883450-T-C

92770243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883445-T-C

92770243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883445-T-G

http://identifiers.org/hco/12/GRCh38#92770349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95883365-C-A

92770349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883365-C-T

http://identifiers.org/hco/12/GRCh38#92770367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95883347-A-C

92770367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883347-A-G

92770367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883347-A-T

http://identifiers.org/hco/12/GRCh38#92770441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95883303-C-A

92770441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883303-C-T

92770579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883209-A-G

92770637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883157-A-G

92770657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883137-G-C

92770657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883137-G-T

http://identifiers.org/hco/12/GRCh38#92770818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95882971-A-C

http://identifiers.org/hco/12/GRCh38#92770980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95882846-C-A

92770992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882834-G-T

92771013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882828-G-A

92771554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882235-A-T

92771689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882102-A-G

http://identifiers.org/hco/12/GRCh38#92772223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881668-A-C

92772306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95881574-T-C

http://identifiers.org/hco/12/GRCh38#92772415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33829
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881463-A-C