178478878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3 prime UTR variant
orthologous variants: 156962733-G-T

178479282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3 prime UTR variant
orthologous variants: 156962219-A-G

http://identifiers.org/hco/1/GRCh38#178479373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156962146-A-C

178479373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3 prime UTR variant
orthologous variants: 156962146-A-G

178479752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156961673-G-A

178479752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156961673-G-T

178481331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156960784-G-T

http://identifiers.org/hco/1/GRCh38#178481892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156960513-A-C

178481892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156960513-A-T

178481988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156960442-C-T

http://identifiers.org/hco/1/GRCh38#178482622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156959687-C-A

http://identifiers.org/hco/1/GRCh38#178482680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156959636-C-A

178482842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156959465-T-C

178482845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156959462-T-A

178483014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156959282-G-T

http://identifiers.org/hco/1/GRCh38#178483313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156959006-C-A

178483313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156959006-C-T

http://identifiers.org/hco/1/GRCh38#178483356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156958963-C-A

178483381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958938-A-G

178483552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958809-A-G

178483626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958727-T-C

178483661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958687-G-A

178483661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958687-G-T

178483662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958686-G-T

178483748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958631-G-A

178483782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958587-G-A

http://identifiers.org/hco/1/GRCh38#178483846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156958506-C-A

178484127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156958036-A-G

178484152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156957986-G-A

178484244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156957881-G-T

178484305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156957826-C-T

178485560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156957061-G-A

178485570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156957051-C-G

178485728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156956907-A-G

178485899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156956758-A-G

178486387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156956045-G-A

178486408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156955975-T-A

178486408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156955975-T-C

178486520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156955869-T-C

178486520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156955869-T-G

178486630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156955759-A-G

178486846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156955618-A-T

178486906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156955558-G-T

http://identifiers.org/hco/1/GRCh38#178486926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156955538-C-A

178486926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156955538-C-T

178487027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954747-G-T

178487029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954745-G-A

178487034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954740-C-T

178487131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954619-G-T

178487229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954518-T-G

http://identifiers.org/hco/1/GRCh38#178487250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156954496-C-A

178487271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954475-G-C

178487410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156954407-T-A

178487796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156954173-T-G

178488174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953981-C-T

http://identifiers.org/hco/1/GRCh38#178488455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156953686-C-A

178488455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953686-C-T

http://identifiers.org/hco/1/GRCh38#178488456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156953685-C-A

178488456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953685-C-T

178488554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156953586-A-G

178488636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953508-G-A

178488636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953508-G-T

178488757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953419-A-G

178488920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953254-G-A

178488932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156953243-A-T

http://identifiers.org/hco/1/GRCh38#178490007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156952661-A-C

http://identifiers.org/hco/1/GRCh38#178490010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156952658-C-A

178490199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156952490-G-A

178490274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156952415-A-G

178490374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156952318-G-A

178490374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156952318-G-T

178490407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156952285-A-T

178490442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 156952250-G-T

178490456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156952236-G-A

178490456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156952236-G-T

http://identifiers.org/hco/1/GRCh38#178490658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156952087-A-C

178490925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951906-C-G

178491191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951680-C-T

http://identifiers.org/hco/1/GRCh38#178491236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156951650-C-A

178491236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951650-C-T

178491360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951529-C-G

178491420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951472-C-G

178491423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951446-A-G

178491691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156951066-A-G

http://identifiers.org/hco/1/GRCh38#178491704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156951054-C-A

178491794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950963-T-C

178491920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950825-T-C

178491956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950806-G-A

178492482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950617-A-G

178492521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156950576-A-G

178492754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950369-G-A

178492789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950336-T-G

178492861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950285-G-A

178492934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156950195-G-T

178493192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949943-C-T

178493277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949876-C-T

178493327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949828-C-T

178493329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949826-A-G

178493367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949793-A-G

178493394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949766-A-G

178493407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949753-G-T

178493459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949703-T-C

178493545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949618-A-G

http://identifiers.org/hco/1/GRCh38#178493553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156949610-C-A

178493553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156949610-C-T

178493588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949586-G-T

http://identifiers.org/hco/1/GRCh38#178493649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156949534-C-A

178493649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156949534-C-T

178493653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949530-G-T

http://identifiers.org/hco/1/GRCh38#178493657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156949526-C-A

178493657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949526-C-T

178493680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949506-C-G

178493709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156949477-G-T

178493710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156949476-A-G

http://identifiers.org/hco/1/GRCh38#178493791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156949400-C-A

http://identifiers.org/hco/1/GRCh38#178493800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156949391-C-A

178494427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156949024-A-G

178494488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156948963-G-A

178494488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156948963-G-T

178494568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 156948883-G-A

178494600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156948851-C-T

178494642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156948809-C-T

http://identifiers.org/hco/1/GRCh38#178494648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156948803-C-A

178494834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156948605-G-A

178494834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156948605-G-T

178494892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156948543-G-A

http://identifiers.org/hco/1/GRCh38#178494907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#156948534-C-A

178494907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156948534-C-G

178494907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 156948534-C-T

http://identifiers.org/hco/1/GRCh38#178494911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156948530-C-A

178494911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156948530-C-T

178495056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant, start_lost, undefined
orthologous variants: 156948424-A-G

178495230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156948320-C-T

178495261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 156948285-A-G

178495423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156948125-T-C

178495697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156947904-A-G

178495747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156947872-A-G

http://identifiers.org/hco/1/GRCh38#178495843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947772-C-A

178495843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156947772-C-G

178495885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156947736-A-G

178495901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947720-G-A

178495921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947699-T-C

178495966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947661-A-G

178495983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947644-G-A

178495984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947643-G-A

178495984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947643-G-T

178496025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947606-G-A

178496025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947606-G-T

http://identifiers.org/hco/1/GRCh38#178496056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947578-C-A

178496056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947578-C-T

http://identifiers.org/hco/1/GRCh38#178496181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947363-A-C

178496181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947363-A-G

178496182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947362-G-A

178496182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947362-G-T

178496303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947270-G-A

178496303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947270-G-C

178496303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947270-G-T

http://identifiers.org/hco/1/GRCh38#178496378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947190-C-A

178496378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947190-C-T

178496452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947096-T-G

178496457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947091-G-T

178496468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947078-T-C

178496468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947078-T-G

178496474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947072-T-A

178496474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947072-T-C

http://identifiers.org/hco/1/GRCh38#178496508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947017-C-A

http://identifiers.org/hco/1/GRCh38#178496513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156947002-C-A

178496513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156947002-C-T

178496713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156946713-T-A

178496726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 156946700-G-T

178496786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946641-T-C

178496794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946632-C-T

178496855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946603-G-A

178496857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946601-G-A

178496857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946601-G-C

178496857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946601-G-T

178496870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946588-G-A

178496870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946588-G-T

178496884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946574-G-T

178496885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946573-G-A

178496885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946573-G-C

178496885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946573-G-T

178496997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156946490-G-A

178496997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 156946490-G-T

178497058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946455-T-C

http://identifiers.org/hco/1/GRCh38#178497088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156946426-C-A

178497088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946426-C-T

178497100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156946414-A-G

178497150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156946385-G-A

178497150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156946385-G-T

178497169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156946367-T-A

178497169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156946367-T-G

http://identifiers.org/hco/1/GRCh38#178498153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156946014-C-A

http://identifiers.org/hco/1/GRCh38#178498270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156945920-C-A

178498621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156945898-A-G

http://identifiers.org/hco/1/GRCh38#178498806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#156945629-C-A

178498806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156945629-C-T

178498992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156945432-C-T

178499231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34521
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156945164-G-A