http://identifiers.org/hco/4/GRCh38#3244287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070133-C-A

3244287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070133-C-T

http://identifiers.org/hco/4/GRCh38#3244297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070143-C-A

3244341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070180-G-A

3244341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070180-G-T

http://identifiers.org/hco/4/GRCh38#3244406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070262-C-A

3244454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070302-C-T

http://identifiers.org/hco/4/GRCh38#3244488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070335-C-A

3244488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070335-C-T

3244504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070341-G-A

3244504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070341-G-T

3244506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070343-T-C

3244507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070344-G-A

3244507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070344-G-T

http://identifiers.org/hco/4/GRCh38#3244582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070425-C-A

3244691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070484-A-G

3244845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35070618-G-A

3244845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35070618-G-T

3244888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35070659-C-T

3244900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35070671-A-G

3245000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 35070818-A-G

http://identifiers.org/hco/4/GRCh38#3245030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35070864-C-A

3245030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070864-C-T

3245034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070868-T-C

3245044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35070948-G-T

3245047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071002-A-G

3245078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071033-G-A

3245078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071033-G-T

3245123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071068-A-G

http://identifiers.org/hco/4/GRCh38#3245223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35071144-C-A

3245262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071168-T-C

http://identifiers.org/hco/4/GRCh38#3245368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35071258-C-A

3245368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: 35071258-C-T

3245431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 35071318-C-T

3245509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35071384-A-G

3245810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35071615-G-T

3245818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35071623-G-A

3245980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35071781-C-G

3245980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35071781-C-T

3246246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35072031-G-A

3246303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35072076-C-G

3246370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35072153-G-T

3246447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35072205-A-G

http://identifiers.org/hco/4/GRCh38#3246603-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35072375-A-C

3246720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35072497-G-A

3246720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35072497-G-T

3246725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35072502-A-G

3247137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35072894-A-T

3247406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073189-G-T

3247490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073277-G-T

3247783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073495-A-G

3248000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073728-G-A

3248000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073728-G-T

3248017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073745-G-A

3248020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073748-G-A

3248020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073748-G-C

3248020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073748-G-T

3248201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073982-G-A

3248206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35073987-C-T

3248396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074104-T-C

http://identifiers.org/hco/4/GRCh38#3248448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074164-C-A

3248448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074164-C-G

3248448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074164-C-T

http://identifiers.org/hco/4/GRCh38#3248468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074183-C-A

3248468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074183-C-T

3248478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074193-A-G

http://identifiers.org/hco/4/GRCh38#3248489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074204-C-A

3248489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074204-C-T

3248504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074223-C-T

3248559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074278-T-C

http://identifiers.org/hco/4/GRCh38#3248605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074325-C-A

3248605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074325-C-G

3248605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074325-C-T

3248615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074335-G-A

3248615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074335-G-T

3248616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074336-G-A

3248616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074336-G-T

http://identifiers.org/hco/4/GRCh38#3248621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074341-A-C

3248647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074364-G-A

3248711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074406-G-A

3248711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074406-G-T

3248781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074459-A-G

http://identifiers.org/hco/4/GRCh38#3248783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074461-C-A

3248937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074646-G-A

3248937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron variant
orthologous variants: 35074646-G-T

http://identifiers.org/hco/4/GRCh38#3249021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35074731-C-A

3249021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron_variant, undefined
orthologous variants: 35074731-C-G

3249021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: intron_variant, undefined
orthologous variants: 35074731-C-T

3249179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35074889-G-T

http://identifiers.org/hco/4/GRCh38#3249408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35075125-C-A

3249408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35075125-C-G

3249408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 35075125-C-T

3249488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35075205-G-A

3249488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 35075205-G-T

http://identifiers.org/hco/4/GRCh38#3249489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35075206-C-A

3249489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 35075206-C-T

http://identifiers.org/hco/4/GRCh38#3249556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35075274-C-A

3249615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075319-T-C

3250054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075770-G-A

3250054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075770-G-T

3250243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075895-G-T

3250588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076181-C-T

3250694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076281-C-T

3250743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076346-G-A

3250804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076428-C-T

3251042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076691-G-A

3251171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076865-C-G

3251184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076878-T-A

3251184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076878-T-C

3251188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076882-G-T

3251478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077110-C-T

3251796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077288-T-C

http://identifiers.org/hco/4/GRCh38#3251907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35077397-A-C

3251966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077490-G-T

3251998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077524-T-A

3252007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077533-G-A

3252007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077533-G-T

3252012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077538-T-C

3252040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077572-A-G

3252054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077585-C-T

3252433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077998-G-A

3252433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077998-G-T

3252465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078030-G-T

3252517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078127-G-A

3252535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078143-G-A

3252838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078399-T-C

http://identifiers.org/hco/4/GRCh38#3252848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35078409-A-C

3253064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078582-G-A

3253064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078582-G-T

http://identifiers.org/hco/4/GRCh38#3253324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35078865-C-A

3253324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 35078865-C-T

3253355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078896-G-A

3253355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078896-G-C

3253428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078969-G-A

http://identifiers.org/hco/4/GRCh38#3253442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35078983-C-A

3253442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078983-C-G

3253442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078983-C-T

3253443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078984-G-A

3253443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35078984-G-T

3253502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079044-T-C

3253524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079075-A-G

http://identifiers.org/hco/4/GRCh38#3253533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35079114-C-A

3253533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079114-C-T

3253534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079115-A-G

3253567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079157-G-A

3253567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079157-G-C

3253567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079157-G-T

3253584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079175-G-A

3253584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079175-G-T

http://identifiers.org/hco/4/GRCh38#3253608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35079199-C-A

3253608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079199-C-T

3253652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079241-G-A

3253652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35079241-G-C

3254589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080030-G-C

3254885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080237-C-T

3254899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080248-G-C

3254933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080279-T-C

3255081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080399-G-A

3255261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080530-C-T

http://identifiers.org/hco/4/GRCh38#3255284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35080550-C-A

3255284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080550-C-T

http://identifiers.org/hco/4/GRCh38#3255627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35080660-C-A

3255627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080660-C-T

3255660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080683-G-A

3255660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080683-G-C

3255660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080683-G-T

3255732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 35080729-G-T

http://identifiers.org/hco/4/GRCh38#3255959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35080902-C-A

3255959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 35080902-C-G

3255959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 35080902-C-T

3256005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35080937-G-A

3256005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35080937-G-T

http://identifiers.org/hco/4/GRCh38#3256061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35080969-C-A

3256061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35080969-C-T

http://identifiers.org/hco/4/GRCh38#3256135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35081036-C-A

3256135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081036-C-G

3256135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081036-C-T

3256157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081059-T-C

http://identifiers.org/hco/4/GRCh38#3256196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35081079-C-A

3256196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081079-C-T

http://identifiers.org/hco/4/GRCh38#3256212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35081094-C-A

3256212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081094-C-T

3256293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081173-T-A

3256377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081268-A-G

http://identifiers.org/hco/4/GRCh38#3256454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35081335-C-A

3256454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081335-C-T

3256475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081356-T-C

3256475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081356-T-G

3256482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081363-G-A

3256494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081374-T-A

3256494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081374-T-C

3256548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35081416-A-G

3256617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081466-C-G

3256742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081561-A-G

http://identifiers.org/hco/4/GRCh38#3256873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35081662-C-A

3256875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081664-G-T

3257030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081770-C-T

3257049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081789-C-T

3257262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081957-G-A

3257618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082239-T-C

3258040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082578-C-T

3258122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082680-G-A

3258179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082739-C-G

3258179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082739-C-T

3258525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35082978-G-T

3259315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083424-G-A

3259356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083462-T-C

3259383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083489-A-G

3259509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083600-C-T

3260233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084323-A-G

3269786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35088937-T-A

3269786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35088937-T-C

3269873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089025-G-T

3269876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089028-G-A

3269876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089028-G-T

http://identifiers.org/hco/4/GRCh38#3269904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089057-C-A

3269904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089057-C-T

3269931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089084-A-G

3269935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089088-C-T

3269938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089090-A-G

3269941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089093-T-C

3270025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089161-G-C

http://identifiers.org/hco/4/GRCh38#3270126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089263-C-A

3270126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089263-C-G

3270126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089263-C-T

http://identifiers.org/hco/4/GRCh38#3270193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089335-C-A

3270193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089335-C-T

http://identifiers.org/hco/4/GRCh38#3270202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089345-C-A

3270202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089345-C-T

3270280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089415-G-A

3270280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089415-G-T

3270304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089441-A-G

3270319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089456-A-G

3270321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089458-A-G

3270372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 35089499-A-G

http://identifiers.org/hco/4/GRCh38#3270394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089514-C-A

3270394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089514-C-T

3270440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089543-G-A

3270440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089543-G-T

http://identifiers.org/hco/4/GRCh38#3270456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089559-C-A

http://identifiers.org/hco/4/GRCh38#3270496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35089601-C-A

3270512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089616-T-A

3270512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089616-T-C

3270731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089702-G-A

3270752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33741
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 35089721-T-C