37983308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3 prime UTR variant
orthologous variants: 157824075-T-G

37983359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3 prime UTR variant
orthologous variants: 157824125-G-A

37983359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3 prime UTR variant
orthologous variants: 157824125-G-T

37983378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3 prime UTR variant
orthologous variants: 157824141-A-G

37983543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense variant
orthologous variants: 157824281-G-T

37983670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157824409-G-A

37983670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157824409-G-T

http://identifiers.org/hco/20/GRCh38#37983908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157824631-C-A

37985302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826372-T-G

37985422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826491-G-T

37985465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826536-T-A

37985465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826536-T-C

37985491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826559-G-A

http://identifiers.org/hco/20/GRCh38#37985947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157826706-C-A

37985947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826706-C-T

37986228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157826983-T-C

37986356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157827060-G-A

37986356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157827060-G-C

37986390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron variant
orthologous variants: 157827063-C-T

http://identifiers.org/hco/20/GRCh38#37986545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157827206-C-A

37986545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157827206-C-T

37987002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 157827696-G-T

37987041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 157827735-T-C

37987056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 157827750-A-G

37987384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157828012-T-C

37987390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157828023-G-A

37987407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157828039-T-C

http://identifiers.org/hco/20/GRCh38#37987450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157828083-C-A

37987450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157828083-C-T

http://identifiers.org/hco/20/GRCh38#37987540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157828172-C-A

37987902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 157828538-T-A

http://identifiers.org/hco/20/GRCh38#37988373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157828939-C-A

37988797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 157829338-A-G

37988932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157829445-T-C

37988934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157829447-T-C

37989068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157829580-C-T

37989273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157829787-T-C

37989273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157829787-T-G

http://identifiers.org/hco/20/GRCh38#37989328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157829838-C-A

37989539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830024-C-T

37989596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830070-C-T

37989708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830152-G-A

37991258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830751-G-A

37991385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830879-C-T

37991398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157830891-A-T

37991637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157831131-T-C

http://identifiers.org/hco/20/GRCh38#37993189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157832103-C-A

37993462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832355-T-G

37993502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832396-G-A

37993624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832483-T-A

37993648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832502-G-A

37993746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832570-G-A

37993891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832724-G-A

37994012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832829-C-T

37994016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832833-C-T

37994048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832863-G-A

37994380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157832935-G-A

37994527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157833006-T-C

37994622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157833105-T-C

37994839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157833328-C-T

37994907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157833395-G-C

37994966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157833454-T-A

http://identifiers.org/hco/20/GRCh38#37995044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157833651-C-A

37995044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157833651-C-G

http://identifiers.org/hco/20/GRCh38#37995545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157834105-C-A

37995545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157834105-C-T

http://identifiers.org/hco/20/GRCh38#37995702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157834265-A-C

37995762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157834318-G-A

37995848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157834382-C-T

http://identifiers.org/hco/20/GRCh38#37996525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157835039-C-A

http://identifiers.org/hco/20/GRCh38#37996596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157835114-C-A

37996596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835114-C-G

37996596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835114-C-T

37996602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835122-A-G

http://identifiers.org/hco/20/GRCh38#37996624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157835151-C-A

37996624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835151-C-T

37996771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157835296-G-A

37996771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157835296-G-C

37996771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157835296-G-T

37997251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835776-T-A

37997290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157835837-T-A

37997764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157836299-G-A

37998379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157836593-C-G

37999047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837171-G-A

37999047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837171-G-C

37999047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837171-G-T

37999227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157837340-G-A

37999227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157837340-G-C

37999227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157837340-G-T

37999255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157837368-T-C

37999312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157837425-T-C

37999379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837488-T-C

http://identifiers.org/hco/20/GRCh38#37999419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157837527-C-A

37999419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837527-C-T

37999437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837560-G-A

37999437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837560-G-C

37999437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837560-G-T

37999525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837685-G-C

37999525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837685-G-T

37999633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157837765-G-C

37999802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157838003-G-T

37999888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157838076-T-C

http://identifiers.org/hco/20/GRCh38#38000452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157838555-C-A

38000452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 157838555-C-T

http://identifiers.org/hco/20/GRCh38#38002476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#157838851-C-A

38002689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157839058-A-G

38002791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 157839157-C-T

38004184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157839823-C-T

38004391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157839994-G-A

http://identifiers.org/hco/20/GRCh38#38004497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157840078-C-A

38004497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157840078-C-T

38004508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157840089-A-G

38004579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157840167-C-T

38005241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157841577-G-A

38005907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157842161-G-A

38005907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157842161-G-T

38006025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157842390-T-C

38006025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157842390-T-G

38006130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157842474-T-C

http://identifiers.org/hco/20/GRCh38#38006170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157842511-C-A

http://identifiers.org/hco/20/GRCh38#38006191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157842534-A-C

38006191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 157842534-A-T

38006224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157842567-T-C

38006246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157842589-T-G

38006273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157842616-G-A

38006273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157842616-G-C

38006273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157842616-G-T

38006296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157842636-T-C

38006296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157842636-T-G

38006456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842783-A-G

38006475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842802-T-C

http://identifiers.org/hco/20/GRCh38#38006519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157842850-C-A

38006519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842850-C-G

38006519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842850-C-T

http://identifiers.org/hco/20/GRCh38#38006531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157842881-C-A

38006547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842897-T-C

38006570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842920-T-C

38006611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842962-G-A

38006616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842967-C-G

38006616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157842967-C-T

38007571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157843536-G-C

38007603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157843567-A-G

38007634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157843588-T-C

38008844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157845428-T-C

38008978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157845610-A-T

38009234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157846038-G-T

38009850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157846640-C-T

38009935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157846724-T-C

38010210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157846990-C-T

http://identifiers.org/hco/20/GRCh38#38011378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157848811-C-A

38011378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157848811-C-T

38011427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157848860-A-G

38011639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157849063-T-C

38011655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849079-A-G

38011674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849098-T-C

38011674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849098-T-G

http://identifiers.org/hco/20/GRCh38#38011697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157849121-C-A

38011697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849121-C-T

38012044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157849468-G-A

38012139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849560-T-A

38012139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849560-T-C

38012151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849572-T-C

38012158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157849579-C-G

38012158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 157849579-C-T

http://identifiers.org/hco/20/GRCh38#38012385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157849806-A-C

38012385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157849806-A-G

38012950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 157850371-G-C

38013337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157850758-G-A

38013337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157850758-G-C

http://identifiers.org/hco/20/GRCh38#38013448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157850869-C-A

38013481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157850902-A-G

38013652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157851073-A-G

38013685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 157851106-G-C

38013723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 157851144-G-C

38013924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157851336-A-G

38013936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157851348-G-T

38014215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157851562-T-C

38014428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157851736-C-T

38014434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157851742-T-C

38014639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157851934-A-T

38014915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157852187-C-T

38015010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157852296-G-C

http://identifiers.org/hco/20/GRCh38#38015340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157852560-C-A

38015390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157852601-C-T

38015833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853172-C-T

38015881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853254-G-A

38016263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853482-C-T

38016312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853531-G-A

38016424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853660-G-A

38016457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853771-T-C

38016475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157853802-A-G

38016728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157854097-G-C

38016728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 157854097-G-T

38021801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859020-G-A

38022223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859511-C-T

38022228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859524-G-A

38022301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859580-C-G

38022337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859615-T-C

38022530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859811-G-T

38022567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859849-G-A

38022589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859871-T-C

38022626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157859900-C-T

38023011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157860389-T-C

38023011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157860389-T-G

38023072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157860440-A-G

38023088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157860464-T-C

38031072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868231-C-T

http://identifiers.org/hco/20/GRCh38#38031087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157868246-C-A

38031111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868270-C-T

38031177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868326-T-G

38031209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868366-C-G

38031431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868615-T-C

38031638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868838-C-T

38031790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157868995-C-G

38031993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157869254-C-T

http://identifiers.org/hco/20/GRCh38#38032150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157869442-A-C

38032154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157869446-C-T

38032217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157869511-C-T

38032808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157869862-G-A

38033268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157870165-G-A

38033268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157870165-G-T

38033277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157870176-A-G

38033335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 157870229-C-T

http://identifiers.org/hco/20/GRCh38#38033354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#157870248-C-A

38033354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157870248-C-T

38033368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29029
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 157870263-C-T