39799010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107580-G-T

39799028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107598-T-C

39799078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107647-G-A

39799115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107684-A-G

39799154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107721-A-G

39799234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107799-G-T

39799250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107815-A-G

http://identifiers.org/hco/15/GRCh38#39799362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118107932-C-A

39799362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107932-C-T

39799363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107933-A-G

39799425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118107995-C-T

http://identifiers.org/hco/15/GRCh38#39799445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118108013-C-A

39799767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108309-C-T

39799842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108388-C-T

39799863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108412-G-T

39799898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108443-A-G

39800059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108563-A-T

39800266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108780-T-C

39800369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108889-G-C

39800442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108959-G-A

39800442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118108959-G-C

http://identifiers.org/hco/15/GRCh38#39800499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118109011-C-A

39800509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109014-T-C

39800513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109018-G-A

39800548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109053-T-C

39800561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109066-A-G

39800561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109066-A-T

39800800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109444-C-T

http://identifiers.org/hco/15/GRCh38#39800866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118109487-A-C

39800866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109487-A-G

http://identifiers.org/hco/15/GRCh38#39800877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118109498-C-A

39800911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109515-T-C

39800919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109523-T-C

39801017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109621-G-C

39801017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109621-G-T

39801030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109634-A-T

http://identifiers.org/hco/15/GRCh38#39801063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118109660-C-A

39801063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 3 prime UTR variant
orthologous variants: 118109660-C-T

39801150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: synonymous variant
orthologous variants: 118109728-A-G

39801420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: synonymous variant
orthologous variants: 118109998-G-A

39801420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: synonymous variant
orthologous variants: 118109998-G-C

39801807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118110388-C-G

39801807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118110388-C-T

39801909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 118110490-G-A

39802077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118110658-G-T

http://identifiers.org/hco/15/GRCh38#39802101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118110682-C-A

39802101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 118110682-C-T

39802338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118110924-G-T

39802390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118110959-A-G

39802754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118111360-C-T

39803826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118111952-G-A

http://identifiers.org/hco/15/GRCh38#39803938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118112065-C-A

http://identifiers.org/hco/15/GRCh38#39803954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118112081-A-C

39803954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118112081-A-G

39804074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118112199-T-C

39804104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118112229-G-C

39804361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118112464-T-C

39804967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113246-C-T

39804989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113269-T-C

39804997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113275-T-C

39805062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113337-A-G

39805072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113346-T-C

39806443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113730-G-A

39806480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113762-G-A

39806505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118113786-C-T

39806854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114035-G-T

39806990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114280-G-A

39806990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114280-G-T

39807140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 118114521-G-A

39807309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114711-T-A

39807448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114814-C-G

39807510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114907-A-G

http://identifiers.org/hco/15/GRCh38#39807522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118114973-C-A

39807522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114973-C-G

39807522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118114973-C-T

39807543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115041-G-A

39807543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115041-G-T

39807599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 118115117-T-C

39807662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115180-C-G

39807681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115199-T-C

39807820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115380-C-G

39807863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115454-A-G

39807888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118115486-G-A

39808366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118116321-G-A

39808534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118116490-T-A

39817139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118121908-G-A

39817241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118122001-G-A

39817393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118122147-G-A

39817486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118122234-G-A

39817832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118123748-T-C

39817917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118123814-G-A

39817948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118123839-A-G

39817981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118123877-A-G

39818065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118123947-C-T

39818346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124240-A-G

39818472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124364-A-G

http://identifiers.org/hco/15/GRCh38#39818576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118124469-C-A

39818612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124503-G-A

39818618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124509-C-T

39818688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124567-C-G

39818688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118124567-C-T

http://identifiers.org/hco/15/GRCh38#39819097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118125189-C-A

39819294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118125367-T-C

39819539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118125982-A-G

39819587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126030-A-G

39819718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126151-G-A

39819718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126151-G-T

39819773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126214-C-T

39819833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126273-C-T

39820063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126499-G-A

39820118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126552-G-A

39820325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118126728-A-T

39820832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127309-G-A

39820884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127361-C-T

39820951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127430-A-T

39820989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127459-G-C

39821138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127612-G-T

39821195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127667-C-T

39821237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127703-A-G

http://identifiers.org/hco/15/GRCh38#39821374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118127840-A-C

39821398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127862-T-C

39821461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118127924-T-G

39821676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118128128-A-G

39821802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118128246-A-T

39821822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118128265-T-C

39822419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118131935-G-C

39822572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118132025-A-G

39822592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118132047-T-C

39822876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118132283-A-T

39826738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118138493-T-G

39826783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118138542-C-T

39827783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139516-C-T

39827998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139683-C-T

39828135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118139996-T-C

39828247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140104-C-G

39828302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140178-C-T

39828439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140334-C-T

39828482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140374-A-T

39828512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118140404-C-G

39828670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118142282-G-A

39828697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118142309-T-C

39828921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118142847-T-C

39829032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118142961-C-T

39829132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118143043-T-C

39829134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118143045-G-A

39829134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118143045-G-T

39829172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118143082-G-T

http://identifiers.org/hco/15/GRCh38#39829215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118143123-A-C

39829304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143201-A-G

39829341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143238-T-C

39829376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143262-C-T

39829387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143272-G-A

39829387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143272-G-T

39829388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143273-G-C

39829388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143273-G-T

http://identifiers.org/hco/15/GRCh38#39829391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118143276-A-C

39829399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143284-G-A

39829399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143284-G-T

http://identifiers.org/hco/15/GRCh38#39829401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118143286-A-C

39829401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143286-A-G

39829402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143287-A-G

39829421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143304-G-T

39829449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143332-C-T

39829459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143342-A-G

39829560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143422-A-G

39829611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143475-T-C

39829696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143561-G-A

39829837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118143771-T-A

39830120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118144154-A-G

http://identifiers.org/hco/15/GRCh38#39830726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118144811-A-C

39832878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146671-G-T

39832981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146767-A-G

http://identifiers.org/hco/15/GRCh38#39833181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118146957-C-A

39833181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118146957-C-T

39833241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118147014-G-A

http://identifiers.org/hco/15/GRCh38#39833431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118147195-A-C

39833431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118147195-A-G

39833476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118147240-T-A

39833763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118147497-T-C

http://identifiers.org/hco/15/GRCh38#39843483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118149088-C-A

39843709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149308-T-C

39843770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149382-A-G

39843826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149439-C-T

39843835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149449-T-C

39843935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149536-A-G

39843939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149541-T-C

39843951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149553-T-C

http://identifiers.org/hco/15/GRCh38#39850498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118149768-C-A

39850498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149768-C-G

39850540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149794-G-A

39850540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118149794-G-T

39850952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118150373-G-A

39851097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118150496-T-C

39851101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118150500-G-A

http://identifiers.org/hco/15/GRCh38#39851289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118150655-A-C

39851413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118150754-T-C

39851692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151057-C-T

39851853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151217-A-T

39852133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118151455-G-T

39852249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118152575-C-G

39852614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118152906-A-G

http://identifiers.org/hco/15/GRCh38#39860688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118154188-C-A

http://identifiers.org/hco/15/GRCh38#39860820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#118154292-C-A

39860820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 118154292-C-G

http://identifiers.org/hco/15/GRCh38#39860869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118154340-C-A

39860873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118154344-G-A

39860873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118154344-G-T

39860886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118154357-C-T

http://identifiers.org/hco/15/GRCh38#39861002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118154483-C-A

39861002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118154483-C-T

39861003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118154484-T-C

39861609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118155714-G-A

39861930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118155960-C-T

39862176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118156308-T-C

39862215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118156339-G-A

39862215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118156339-G-T

39862265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118156387-T-C

39862273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118156395-G-T

http://identifiers.org/hco/15/GRCh38#39862357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118156473-A-C

39862377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118156496-T-C

39862377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118156496-T-G

39862387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118156506-G-A

39862387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118156506-G-T

http://identifiers.org/hco/15/GRCh38#39862392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118156511-C-A

http://identifiers.org/hco/15/GRCh38#39862462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118156579-A-C

39867502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118159942-A-T

39868138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118160690-C-T

http://identifiers.org/hco/15/GRCh38#39868407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118160993-C-A

39868686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161262-T-C

39868814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161368-G-A

39868814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161368-G-T

39868867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161413-C-T

39869094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161572-C-T

39869275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161675-G-A

39869410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161799-G-A

39869564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118161940-C-T

http://identifiers.org/hco/15/GRCh38#39869565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118161941-A-C

39869636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162008-C-T

39869682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162040-G-T

39869991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162309-G-T

http://identifiers.org/hco/15/GRCh38#39870083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118162373-C-A

39870083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162373-C-T

39870158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162439-C-T

39870838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162666-T-G

39871129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118162926-C-G

39871234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163037-G-A

39871488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163452-T-A

39871513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163470-C-T

39871743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163715-A-G

39871877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163821-T-C

39872015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118163959-A-G

39872239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118164168-T-C

39872243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118164172-G-A

http://identifiers.org/hco/15/GRCh38#39872337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118164238-C-A

39872337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118164238-C-T

39872408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118164300-G-A

39873560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165042-G-A

39873560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165042-G-T

39873692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165152-G-C

39873867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165309-T-C

http://identifiers.org/hco/15/GRCh38#39874122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118165510-A-C

39874177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165545-T-C

39874337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118165701-T-G

39874497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166215-T-A

39874595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166333-G-T

39874760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166474-C-T

39874833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166534-C-G

39874833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166534-C-T

39875102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118166717-T-A

39875475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167031-G-A

39875491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167047-C-T

39875589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167143-G-C

39875639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167185-G-A

39875655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167201-G-T

39876063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118167921-A-G

http://identifiers.org/hco/15/GRCh38#39877055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118168871-C-A

39877055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118168871-C-T

39877298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118169114-C-G

http://identifiers.org/hco/15/GRCh38#39877508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118169630-A-C

http://identifiers.org/hco/15/GRCh38#39880500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118169832-A-C

http://identifiers.org/hco/15/GRCh38#39880622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118169934-C-A

39880622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118169934-C-G

39880865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170128-G-A

39880865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170128-G-T

39880884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170150-T-C

http://identifiers.org/hco/15/GRCh38#39881016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118170280-C-A

http://identifiers.org/hco/15/GRCh38#39881027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118170291-C-A

39881085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170339-C-T

39881137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170402-T-C

39881153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170418-C-T

39881154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170419-A-G

39881272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170532-T-G

39881372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118170621-T-A

39881655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171130-T-C

39881982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171482-T-G

39882100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171606-G-A

39882205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171712-C-T

39882209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118171716-T-C

39882654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172137-A-G

http://identifiers.org/hco/15/GRCh38#39882655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118172138-C-A

39882722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172196-G-A

39882765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172245-T-C

39882807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172283-C-T

http://identifiers.org/hco/15/GRCh38#39882887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118172376-C-A

39882936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172520-T-C

39883066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172651-A-G

39883190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172738-A-G

39883254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172800-T-A

39883370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172922-G-A

39883388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118172945-A-G

39883452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118173017-T-C

39883548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118173090-C-T

39883556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118173098-T-A

http://identifiers.org/hco/15/GRCh38#39883711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118174151-A-C

39883763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118174201-A-G

http://identifiers.org/hco/15/GRCh38#39883891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118174326-A-C

39883898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118174333-A-G

http://identifiers.org/hco/15/GRCh38#39884080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118174500-C-A

39884080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118174500-C-T

39884259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118174679-G-A

39884421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118174847-A-G

39884641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118175033-T-C

http://identifiers.org/hco/15/GRCh38#39884755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118175112-C-A

39885070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118175410-G-T

39888772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118179356-C-T

39888907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118179473-T-A

39889090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118179519-G-C

39889766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118180084-A-G

39890333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118180519-A-G

39891126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118181225-G-T

39896990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118184199-G-A

39897098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118184290-G-T

39898507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118185660-G-C

http://identifiers.org/hco/15/GRCh38#39898745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118185910-A-C

39898745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118185910-A-G

http://identifiers.org/hco/15/GRCh38#39898888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118186050-C-A

39899563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118186627-G-C

39900105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187077-T-A

39900105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187077-T-C

39900109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187081-A-G

39900313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187336-A-G

39900350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187378-G-C

39900787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118187826-A-G

http://identifiers.org/hco/15/GRCh38#39901065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118188081-C-A

http://identifiers.org/hco/15/GRCh38#39901677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118188735-A-C

39901721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118188779-T-G

39902267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118189708-A-G

39902267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118189708-A-T

39902600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118190026-A-G

39902704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118190130-G-T

39905132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118191667-C-T

39905197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118191732-A-G

39905609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118191842-A-G

39905779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118192008-T-C

39905922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118192149-C-T

39906454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118192723-G-A

http://identifiers.org/hco/15/GRCh38#39906622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118192895-A-C

39906622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118192895-A-T

39906996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193232-T-C

39907028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193263-G-A

39907164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193506-T-C

39907379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193708-G-A

39907501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193813-C-T

39907522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193833-C-T

39907535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193846-T-C

39907563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118193875-G-C

http://identifiers.org/hco/15/GRCh38#39907742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118194026-C-A

39907742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118194026-C-T

39908803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118194914-T-A

39908810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118194921-C-T

39908911-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195019-A-T

39908916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195024-C-T

39908950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195056-T-C

39909918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195182-T-A

39909918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195182-T-C

39910005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118195264-G-T

39914629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199129-C-G

39914629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199129-C-T

39914649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199150-G-T

39914669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199169-T-A

39915098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199857-C-T

39915099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199858-A-G

39915199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118199975-T-C

39915750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

39915750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

39915871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/15/GRCh38#39915987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

39916146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

39916266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118200840-T-C

http://identifiers.org/hco/15/GRCh38#39916289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118200864-A-C

39916494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201052-G-A

39916543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201086-A-G

39916665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201202-T-C

39916960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201471-A-T

39918084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201622-C-T

39918098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201639-A-G

39918387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118201922-T-C

http://identifiers.org/hco/15/GRCh38#39918439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118201992-A-C

39918952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118202512-T-C

39919220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118202898-T-G

39919272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118202945-G-A

39919583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118203275-G-A

39919583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118203275-G-C

39919635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118203327-G-A

39919835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118203478-G-A

39919835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118203478-G-T

http://identifiers.org/hco/15/GRCh38#39919841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118203485-C-A

39919841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118203485-C-G

39919841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118203485-C-T

39920094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203734-C-T

39920193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203834-G-A

39920193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203834-G-T

39920259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118203898-G-A

39920269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118203908-G-A

39920269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118203908-G-T

http://identifiers.org/hco/15/GRCh38#39920274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118203913-C-A

39920274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118203913-C-T

39920293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203925-G-A

39920293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203925-G-C

39920293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118203925-G-T

39920379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204006-A-G

39920529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204079-G-C

39920591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118204143-C-T

39920602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118204154-G-C

39920620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204170-G-A

39920620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204170-G-T

39920621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204171-A-G

http://identifiers.org/hco/15/GRCh38#39920672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118204218-C-A

39920672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204218-C-G

http://identifiers.org/hco/15/GRCh38#39920699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#118204248-C-A

39920699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118204248-C-G

39920699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 118204248-C-T

39920712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204268-T-C

39920733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204277-T-A

39920733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204277-T-G

http://identifiers.org/hco/15/GRCh38#39920771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118204298-C-A

39920771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204298-C-T

http://identifiers.org/hco/15/GRCh38#39920809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#118204335-C-A

39920809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204335-C-T

39920840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204373-G-A

39920840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204373-G-T

39920895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204432-G-T

39920896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204433-G-A

39920925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204462-G-A

39920925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32370
most severe consequence: 5 prime UTR variant
orthologous variants: 118204462-G-T