156894682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87675399-C-G

156895076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87675080-A-G

http://identifiers.org/hco/1/GRCh38#156896675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#87674366-C-A

156896675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 87674366-C-G

http://identifiers.org/hco/1/GRCh38#156897689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87673254-A-C

156898209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87672713-G-A

156899239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87672201-A-G

156900222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87671414-T-C

156900273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87671374-T-A

156900274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87671373-C-G

156900338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87671317-C-T

http://identifiers.org/hco/1/GRCh38#156900496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87671151-C-A

156900496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87671151-C-T

http://identifiers.org/hco/1/GRCh38#156900607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87671075-A-C

156900711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87670971-G-A

156901163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87670631-T-C

156901164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87670630-G-A

156901247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87670548-C-T

156902059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669840-G-C

156902059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669840-G-T

156902066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669833-G-T

http://identifiers.org/hco/1/GRCh38#156902148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87669626-C-A

156902148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669626-C-T

156902308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669504-A-G

156902314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669498-A-G

156902392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669432-G-A

156902392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87669432-G-T

156902781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 87669069-G-A

http://identifiers.org/hco/1/GRCh38#156903776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87667766-C-A

156903819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87667728-T-C

http://identifiers.org/hco/1/GRCh38#156903867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87667680-C-A

156903900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 87667646-G-A

156904086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667506-T-C

http://identifiers.org/hco/1/GRCh38#156904153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87667484-C-A

156904173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667468-T-C

156904344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667343-T-C

156904508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667103-G-A

http://identifiers.org/hco/1/GRCh38#156904555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87667058-C-A

156904555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667058-C-T

http://identifiers.org/hco/1/GRCh38#156904632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87667001-C-A

156904632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87667001-C-T

156904664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666971-G-A

156904664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666971-G-T

156904678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666955-G-T

http://identifiers.org/hco/1/GRCh38#156904686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87666947-C-A

156904686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666947-C-T

156904689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666943-G-A

156904701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666931-C-T

156904719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666913-C-G

156904719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666913-C-T

156904754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 87666880-T-C

156904832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 87666802-C-T

http://identifiers.org/hco/1/GRCh38#156905093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87666615-C-A

156905093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666615-C-G

156905093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666615-C-T

156905220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666537-G-A

156905220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666537-G-T

http://identifiers.org/hco/1/GRCh38#156905367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87666456-C-A

156905367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87666456-C-G

156905389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87666434-G-T

http://identifiers.org/hco/1/GRCh38#156905498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87666339-C-A

http://identifiers.org/hco/1/GRCh38#156905506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87666331-C-A

156905506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666331-C-T

156905585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666252-G-C

156905585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666252-G-T

156905897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666064-C-T

156905901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666060-T-C

156905958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87666008-A-G

156906186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87665806-T-A

156906186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87665806-T-C

156906186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87665806-T-G

http://identifiers.org/hco/1/GRCh38#156906225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87665771-C-A

156906225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87665771-C-G

156906225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87665771-C-T

http://identifiers.org/hco/1/GRCh38#156906386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87665612-C-A

156906485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87665596-A-G

156906528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87665553-A-G

156906545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87665536-G-T

156906583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87665511-G-A

156906718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87665394-G-A

156906858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87665254-C-G

156906858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87665254-C-T

156907021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87665153-T-C

156907311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664864-C-T

156907382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664779-G-A

156907494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664699-G-A

156907494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664699-G-C

156907521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664672-G-A

156907521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664672-G-T

156907571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664606-G-C

156907571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87664606-G-T

156907624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87664555-G-A

156907641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87664538-G-A

156907685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87664494-C-G

156907744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664434-G-A

156907751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664427-G-A

156907788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664389-G-T

156907844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664349-T-G

156907863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87664331-C-T

156907907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87664296-C-T

http://identifiers.org/hco/1/GRCh38#156907908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87664295-C-A

156907908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87664295-C-T

156908063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664145-G-T

156908068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664134-G-A

156908068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664134-G-C

156908068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664134-G-T

156908074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664128-G-A

156908074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87664128-G-T

156908231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663966-T-C

156908276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663921-C-T

156908376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663827-G-T

156908484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663722-G-A

156908484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663722-G-T

http://identifiers.org/hco/1/GRCh38#156908606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87663633-C-A

156908806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663434-T-C

156908806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663434-T-G

http://identifiers.org/hco/1/GRCh38#156908818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87663422-C-A

156908818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663422-C-T

156908854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663386-A-G

156908884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663362-G-A

http://identifiers.org/hco/1/GRCh38#156908885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87663361-C-A

156908885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663361-C-T

156908952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87663294-T-C

156909110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663159-G-C

156909110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87663159-G-T

156909264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87662588-A-T

156909326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87662527-G-A

http://identifiers.org/hco/1/GRCh38#156909739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87661977-C-A

156909739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87661977-C-T

156909743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87661973-T-A

156909743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87661973-T-C

156909834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87661883-G-C

156909846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87661871-A-G

156909855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87661862-A-G

156909912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87661805-C-T

156910000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87661706-T-C

156910152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87661552-C-T

156910470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87661293-C-T

156910603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87661213-A-G

156910738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87661076-C-G

156910738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87661076-C-T

http://identifiers.org/hco/1/GRCh38#156910801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87661018-C-A

156910801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87661018-C-T

156910803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87661016-G-T

156910837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660989-G-T

http://identifiers.org/hco/1/GRCh38#156911669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87660733-C-A

156911669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660733-C-G

156911669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660733-C-T

http://identifiers.org/hco/1/GRCh38#156911697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87660710-C-A

156911717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660690-A-G

156912073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87660282-G-A

156912101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660262-A-G

156912101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660262-A-T

156912137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87660225-T-C

http://identifiers.org/hco/1/GRCh38#156912407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659986-C-A

156912407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659986-C-T

156912434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659962-A-G

156912444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659952-A-G

156912545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87659854-G-T

http://identifiers.org/hco/1/GRCh38#156912658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659744-C-A

156912658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659744-C-T

156912678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659724-G-A

156913046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659363-T-C

156913056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659353-C-T

156913168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659273-A-G

156913177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659264-T-C

156913188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87659253-A-G

http://identifiers.org/hco/1/GRCh38#156913194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659247-A-C

156913194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87659247-A-G

http://identifiers.org/hco/1/GRCh38#156913268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659173-C-A

156913268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87659173-C-T

http://identifiers.org/hco/1/GRCh38#156913313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659128-A-C

http://identifiers.org/hco/1/GRCh38#156913320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659121-C-A

156913320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659121-C-T

http://identifiers.org/hco/1/GRCh38#156913351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87659099-C-A

156913351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87659099-C-T

156913391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 87659078-G-C

http://identifiers.org/hco/1/GRCh38#156913489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#87658977-C-A

156913489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87658977-C-T

156913517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87658961-G-A

156913537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87658941-G-A

http://identifiers.org/hco/1/GRCh38#156913539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87658939-C-A

156913539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87658939-C-T

156913616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87658883-G-A

156913708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87658803-C-T

156913775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658730-G-A

156913775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658730-G-T

156913813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658700-G-T

156914067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87658448-G-A

http://identifiers.org/hco/1/GRCh38#156914088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87658427-C-A

156914088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87658427-C-T

http://identifiers.org/hco/1/GRCh38#156914145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87658363-C-A

156914145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658363-C-T

156914147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658361-A-G

156914188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658331-G-A

156914188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658331-G-T

156914195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658324-G-A

156914205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658317-G-A

156914205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658317-G-T

156914242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658283-G-A

156914242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658283-G-C

156914246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87658279-T-C

156914521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87657718-T-A

156914639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 87657610-G-A

156914668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87657581-A-G

156914673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87657576-C-T

156914763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87657486-C-T

156914874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657417-C-G

156914874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657417-C-T

156914941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657352-G-T

156914972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657320-G-A

156914972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657320-G-T

http://identifiers.org/hco/1/GRCh38#156915005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87657287-C-A

156915087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87657216-A-G

156915091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87657197-G-A

156915101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87657187-T-C

156915163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87657131-G-T

156915395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87656941-A-G

http://identifiers.org/hco/1/GRCh38#156915432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87656915-C-A

156915510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87656867-T-C

156915680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87656720-G-A

156915680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87656720-G-T

http://identifiers.org/hco/1/GRCh38#156915837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33631
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#87656412-C-A