71041799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97649717-C-T

71041862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97649779-T-C

71042022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97649917-C-T

http://identifiers.org/hco/13/GRCh38#71042057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97649953-A-C

71042221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650099-A-G

71042842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650710-C-T

71043044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97650984-C-T

http://identifiers.org/hco/13/GRCh38#71043083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97651017-A-C

71043083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651017-A-T

71043386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651245-G-A

71043386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651245-G-C

71043544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651383-T-C

71043558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651397-T-C

71043572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651411-G-A

71043686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651512-A-T

71043723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651549-C-T

71043934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651752-A-G

71043981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651799-T-A

71044002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651823-C-G

71044002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651823-C-T

71044088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97651908-T-C

71044338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97652144-G-T

71044788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97652782-A-G

71045002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97659608-G-T

http://identifiers.org/hco/13/GRCh38#71045419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97660028-C-A

71045547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97660135-T-A

71045547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97660135-T-C

71045632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97660215-G-C

71045681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97660255-T-C

71050437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97664611-C-T

71050576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97664742-T-C

71074263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97667660-C-T

71074265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97667662-T-C

71074381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97667775-C-G

71074383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97667777-T-G

http://identifiers.org/hco/13/GRCh38#71074505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97667897-C-A

http://identifiers.org/hco/13/GRCh38#71074629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97668027-C-A

71074672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668060-A-G

71074700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668083-C-T

71074799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668143-T-C

http://identifiers.org/hco/13/GRCh38#71074836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97668179-C-A

71074892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668234-G-T

71074999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668357-T-C

71075443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668785-C-T

71075445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668787-T-A

71075572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668912-A-G

71075606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668946-T-C

71075611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97668951-T-C

71075671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669008-C-T

71075749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669095-T-C

71075912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669240-C-T

71075927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669255-C-T

71076082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669396-G-T

71076312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97669641-A-G

71076775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97670110-T-A

71077345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97670639-T-C

71077502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97670794-C-G

71078574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97672878-G-A

71078669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97672983-C-T

71079023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673339-G-A

71079023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673339-G-C

71079023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673339-G-T

71079236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673552-G-C

71079365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673677-A-G

http://identifiers.org/hco/13/GRCh38#71079597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97673864-C-A

71079674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97673949-A-T

71080018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675216-G-A

http://identifiers.org/hco/13/GRCh38#71080060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97675254-C-A

71080060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675254-C-T

71080371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675539-T-C

71080503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675662-G-A

71080503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675662-G-T

71080669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97675827-C-T

71081409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97676436-T-C

71081551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97676571-G-T

71081996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97676940-C-T

71082445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97677288-A-G

71082946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97678076-T-G

71082970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97678100-A-G

http://identifiers.org/hco/13/GRCh38#71083146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97678266-C-A

71083146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97678266-C-G

71083499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97678647-A-T

71083516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97678664-C-T

71084570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97679439-T-C

71084990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97679048-G-A

71089946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97680964-A-G

71089976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97680994-A-G

71090075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681096-A-G

71090075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681096-A-T

71090209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681206-G-T

71090795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681383-C-T

71090808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681396-A-T

71090934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681524-A-G

71090934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681524-A-T

71091040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681629-C-T

71091270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97681860-G-A

71091878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682466-C-T

71092129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682743-G-A

71092232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682840-G-T

71092338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682939-G-T

71092349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682963-T-C

71092358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97682972-A-T

71094100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97684911-T-C

71094103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97684914-T-G

71094182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97684969-G-A

71094193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97684979-G-T

71094295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685078-A-G

71094343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685127-T-C

71094365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685145-A-T

71095835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685824-C-T

71095888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685876-G-C

71096015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97685960-C-T

71096073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686015-T-C

71096265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686144-C-T

71096598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686476-T-A

71096732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686597-G-T

71096858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686723-A-G

71096872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686737-C-G

71096877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97686742-C-T

http://identifiers.org/hco/13/GRCh38#71097012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97686896-A-C

71097271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687124-C-G

http://identifiers.org/hco/13/GRCh38#71097307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97687164-A-C

71097481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687339-G-A

71097494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687352-A-G

71097499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687357-A-G

71097520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687382-A-G

71097520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687382-A-T

71097662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687509-A-G

71097742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687583-A-T

71097860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687699-G-C

71097970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97687807-G-A

71099301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97688044-C-T

71099328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97688072-A-G

71099333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97688077-T-C

71099659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97688397-C-T

71115773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97696764-T-A

71116058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97697082-C-G

71116058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97697082-C-T

71116934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97698967-T-G

71117157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699166-T-G

71117171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699181-C-T

71117245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699258-T-C

71117324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699339-A-T

71117367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699383-C-T

71117407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699422-T-C

71117454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699467-A-G

71117481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699494-T-C

http://identifiers.org/hco/13/GRCh38#71117487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97699500-C-A

71117487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699500-C-G

71117517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97699530-T-G

71118421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97701578-C-G

71118421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97701578-C-T

71118603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97701753-G-A

71118649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97701799-A-G

71119137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97702283-C-T

71123186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97707654-A-T

71124017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97708503-T-A

71124149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97708594-C-G

71124246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97708667-G-A

71124246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97708667-G-C

71124246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97708667-G-T

71124884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97709220-T-G

71124893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97709229-G-T

71135526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714019-A-G

71135628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714135-G-A

71135693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714302-C-T

71135851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714485-C-G

71135911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714532-A-G

71136001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714592-G-A

71136189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714768-A-G

71136189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714768-A-T

http://identifiers.org/hco/13/GRCh38#71136238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97714812-A-C

71136320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97714892-A-G

71136473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97715059-C-G

71137133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97715743-A-G

71137357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97715967-G-A

71137357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97715967-G-T

http://identifiers.org/hco/13/GRCh38#71137520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97716130-C-A

71137579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716189-T-C

71137624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716236-C-T

71137662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716378-G-A

71137681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716445-G-A

71137765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716649-C-G

71137765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716649-C-T

71137974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97716845-T-C

http://identifiers.org/hco/13/GRCh38#71138124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97717023-C-A

71138124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717023-C-G

71138160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717059-G-A

71138167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717060-G-T

71138224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717123-A-G

71138350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717239-T-G

71138377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717256-G-T

71138563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717438-G-A

71138665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717532-G-C

71138809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717669-T-C

71138822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717682-C-T

71138937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97717794-G-T

71140197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97719499-A-G

http://identifiers.org/hco/13/GRCh38#71140224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97719530-A-C

71140256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97719565-G-C

71140256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97719565-G-T

http://identifiers.org/hco/13/GRCh38#71140396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97719676-C-A

71140525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97719805-G-C

71140593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97719872-A-G

71140953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97720216-A-G

http://identifiers.org/hco/13/GRCh38#71141025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97720289-C-A

http://identifiers.org/hco/13/GRCh38#71141034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97720299-C-A

71141034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97720299-C-T

71141100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97720356-T-C

http://identifiers.org/hco/13/GRCh38#71141361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97720475-A-C

71141748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97720642-A-T

71141941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97720830-G-T

71142175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721102-G-A

71142175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721102-G-T

71143957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721370-G-T

71144010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721421-G-T

71144336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721767-A-G

71144381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721799-A-T

71144495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721896-C-G

http://identifiers.org/hco/13/GRCh38#71144577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97721974-A-C

71144577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721974-A-G

71144577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97721974-A-T

71144617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97722011-C-T

71144656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97722030-T-C

71144814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97722179-G-A

71145069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97723471-C-G

71145278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97724414-T-C

71145291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 97724427-T-A

http://identifiers.org/hco/13/GRCh38#71145311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97724447-C-A

71145311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724447-C-T

71145335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724469-T-C

71145398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724524-T-A

71145505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724614-C-T

71145529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724632-G-T

71145741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724823-T-C

71145761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724842-G-A

71145781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97724862-G-A

71146142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725120-T-C

71146259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725234-A-G

71146283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725245-A-G

71146332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725281-T-C

71146332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725281-T-G

71146408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725356-A-G

71146475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725404-G-T

71146689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725510-A-G

http://identifiers.org/hco/13/GRCh38#71146703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97725524-A-C

71146703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725524-A-G

71146705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725526-A-G

71147092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725920-C-T

71148079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97725984-T-A

71148220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726095-A-G

71148267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726142-G-A

71148267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726142-G-T

71148345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726204-T-C

71148345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726204-T-G

71148374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726232-A-G

71149025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97726887-G-C

71149163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727025-A-G

71149254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727117-C-G

71149254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727117-C-T

71149479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727326-G-C

71149479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727326-G-T

71149572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727419-T-C

71149572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727419-T-G

71149863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97727755-G-T

71150127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97728029-G-T

71150148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97728050-C-T

http://identifiers.org/hco/13/GRCh38#71150429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97728331-C-A

71150429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97728331-C-T

71150492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97728394-C-T

71150751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97728620-T-C

71151037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729132-C-T

71151048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729143-A-T

71151083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729180-T-C

71151121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729216-A-T

http://identifiers.org/hco/13/GRCh38#71151196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97729286-A-C

71151196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729286-A-G

71151273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97729352-C-T

http://identifiers.org/hco/13/GRCh38#71151517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97729560-C-A

http://identifiers.org/hco/13/GRCh38#71155405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97730329-A-C

71155405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730329-A-G

71155405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730329-A-T

71155407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730331-T-A

71155429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730350-C-T

71155492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730398-G-C

71155578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730474-T-C

http://identifiers.org/hco/13/GRCh38#71155605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97730499-C-A

71155605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730499-C-G

71155605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730499-C-T

http://identifiers.org/hco/13/GRCh38#71155667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97730559-A-C

71155695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730583-T-C

71155811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730692-T-C

http://identifiers.org/hco/13/GRCh38#71155854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97730742-A-C

http://identifiers.org/hco/13/GRCh38#71155855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97730743-C-A

71155855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730743-C-T

71156222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730874-C-T

71156340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97730956-C-T

http://identifiers.org/hco/13/GRCh38#71156414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97731035-C-A

71156414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731035-C-T

71156451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731070-C-T

71156479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731098-G-A

71156479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731098-G-T

71156530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731152-C-G

71156535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731157-G-T

71156924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731697-G-T

71157002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731785-A-T

71157008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731791-G-T

71157030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731812-A-G

71157032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731814-T-C

71157177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97731963-G-C

71157499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97732290-T-G

http://identifiers.org/hco/13/GRCh38#71158452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97733547-C-A

http://identifiers.org/hco/13/GRCh38#71158488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97733592-A-C

71158488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97733592-A-G

71158725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97733815-A-G

71158800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97733883-C-T

71158812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97733895-T-C

71159217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734269-G-A

71159399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734399-G-A

71159405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734402-T-C

71159658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734652-G-A

71159813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734806-C-T

71159910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97734902-A-G

71160039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97735030-C-T

71160308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97735337-T-G

71160463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97735493-T-C

71160710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97735738-A-G

71160774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97735809-C-G

http://identifiers.org/hco/13/GRCh38#71160829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97735868-A-C

71161026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736056-G-A

71161026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736056-G-T

71161056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736086-G-A

71161120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736139-C-G

71161120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736139-C-T

71161141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736172-G-A

71161230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736627-G-A

71161309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736704-C-T

71161584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736966-T-C

71161614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97736997-C-G

71162858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741410-T-A

71162858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741410-T-C

71162872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741425-T-G

71162886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741440-T-C

http://identifiers.org/hco/13/GRCh38#71162949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97741506-C-A

71164810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741711-T-C

71164816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741717-C-T

71165073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97741977-T-C

71165342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97742230-G-C

71165503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97742389-G-T

71165512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97742429-T-A

71166224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743201-G-T

71166233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743210-A-G

71166323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743293-G-A

71166346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743320-C-T

71166430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743401-C-T

71166511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743481-A-T

71166556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743527-A-G

71166582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743553-C-G

71166582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97743553-C-T

71167143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97747148-T-A

71167206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97747206-G-A

71167239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97747238-C-T

http://identifiers.org/hco/13/GRCh38#71167240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#97747239-C-A

71167240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97747239-C-G

71167363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97747291-C-T

71167381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: non coding transcript exon variant
orthologous variants: 97747309-T-C

71167425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 97747345-A-G

71167611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97747485-G-A

71167883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42658
most severe consequence: non coding transcript exon variant
orthologous variants: 97747719-T-C