12734313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706222-G-A

12734313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706222-G-C

12734313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706222-G-T

12734338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706247-C-T

12734383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706280-C-G

12734433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706328-A-G

12734467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706361-C-T

http://identifiers.org/hco/3/GRCh38#12734492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706384-C-A

12734492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706384-C-T

http://identifiers.org/hco/3/GRCh38#12734502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706394-C-A

12734515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706406-T-C

12734546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706416-T-A

12734546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706416-T-C

http://identifiers.org/hco/3/GRCh38#12734555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706425-C-A

12734555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706425-C-T

12734561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706431-T-C

http://identifiers.org/hco/3/GRCh38#12734606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706466-C-A

12734606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3 prime UTR variant
orthologous variants: 115706466-C-T

http://identifiers.org/hco/3/GRCh38#12734651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706506-C-A

12734651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115706506-C-T

http://identifiers.org/hco/3/GRCh38#12734754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706607-C-A

12734754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115706607-C-T

12734812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706664-A-G

12734812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706664-A-T

http://identifiers.org/hco/3/GRCh38#12734860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706700-C-A

12734860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706700-C-T

http://identifiers.org/hco/3/GRCh38#12734925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115706767-A-C

12734925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706767-A-G

12734925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706767-A-T

12734927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706769-G-A

12734927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115706769-G-T

12735307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707111-A-G

12735375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707167-G-A

http://identifiers.org/hco/3/GRCh38#12735417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707263-A-C

12735417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707263-A-T

12735425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707271-G-T

12735447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707293-G-A

12735447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707293-G-T

12735477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707318-C-G

12735497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707338-T-C

12735580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115707422-G-A

12735580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115707422-G-C

http://identifiers.org/hco/3/GRCh38#12735656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707500-C-A

12735656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707500-C-T

http://identifiers.org/hco/3/GRCh38#12735672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707516-C-A

12735672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707516-C-T

http://identifiers.org/hco/3/GRCh38#12735680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707536-C-A

12735680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707536-C-T

12735687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707543-C-T

12735690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707546-G-A

12735690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707546-G-T

12735692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707548-G-T

http://identifiers.org/hco/3/GRCh38#12735713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707575-C-A

12735713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707575-C-T

http://identifiers.org/hco/3/GRCh38#12735715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707577-C-A

12735733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707594-G-A

12735733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707594-G-C

12735733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707594-G-T

12735792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707642-G-A

12735868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707710-T-C

12736038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707738-T-A

12736166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707849-T-G

12736477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707871-T-A

12736477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707871-T-C

http://identifiers.org/hco/3/GRCh38#12736480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707874-C-A

12736480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707874-C-G

12736480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707874-C-T

12736546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707934-G-C

12736546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707934-G-T

http://identifiers.org/hco/3/GRCh38#12736558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115707948-A-C

12736558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115707948-A-G

12736588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115707978-G-A

12736594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115707984-G-T

http://identifiers.org/hco/3/GRCh38#12736756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115708135-C-A

12736756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115708135-C-T

12736798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 115708180-G-A

12736847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708229-G-C

http://identifiers.org/hco/3/GRCh38#12736946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115708334-C-A

12736954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708342-T-C

12737180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115708609-T-C

12737440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710347-G-A

12737440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710347-G-C

12737440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710347-G-T

http://identifiers.org/hco/3/GRCh38#12737612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115710524-C-A

12737612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115710524-C-T

http://identifiers.org/hco/3/GRCh38#12737645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115710556-A-C

12737645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115710556-A-G

http://identifiers.org/hco/3/GRCh38#12737838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115710723-A-C

http://identifiers.org/hco/3/GRCh38#12737929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115710776-C-A

12737929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710776-C-T

12738002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710848-T-C

12738097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710921-C-T

12738118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710938-T-G

12738120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115710940-G-C

12738211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115711030-G-C

12738211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115711030-G-T

http://identifiers.org/hco/3/GRCh38#12738233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115711052-C-A

12738233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115711052-C-G

12738534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115711752-C-T

12738565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115711783-A-G

12738623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115711839-T-A

12738692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115711906-C-T

http://identifiers.org/hco/3/GRCh38#12738762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115711977-C-A

12738762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115711977-C-T

http://identifiers.org/hco/3/GRCh38#12738775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115711990-A-C

12738775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115711990-A-G

http://identifiers.org/hco/3/GRCh38#12742335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115713236-C-A

12742413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713307-C-T

12742414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713308-G-A

12742414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713308-G-C

12742414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713308-G-T

12742426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713316-T-C

12742658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713493-G-A

12742658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713493-G-T

12742663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115713498-T-A

12743812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115715822-G-T

12743855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115715865-G-A

12743855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115715865-G-T

12743858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115715868-G-A

http://identifiers.org/hco/3/GRCh38#12743884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115715894-A-C

12743904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115715913-T-G

12743918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, missense_variant
orthologous variants: 115715927-G-A

12743918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, missense_variant
orthologous variants: 115715927-G-C

12743918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, missense_variant
orthologous variants: 115715927-G-T

12744045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716035-T-C

12744049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716039-T-G

12744063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716053-C-T

http://identifiers.org/hco/3/GRCh38#12744111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115716087-C-A

12744111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716087-C-T

12744126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716100-T-G

12744359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716278-T-A

http://identifiers.org/hco/3/GRCh38#12744437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115716355-C-A

12744479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716397-G-C

12744536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716424-G-A

12744821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716709-T-A

12744821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115716709-T-G

12744944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115717300-C-T

12748649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718496-C-G

12748649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718496-C-T

12748679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, missense_variant
orthologous variants: 115718520-A-T

12748680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718521-T-C

12748689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718530-T-G

12748692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718533-G-A

12748701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718542-G-C

12748707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718560-G-A

12748716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 115718569-A-G

12748797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 115718637-A-G

http://identifiers.org/hco/3/GRCh38#12748832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115718669-C-A

12748871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718711-T-C

12748932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718763-G-A

12748932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718763-G-T

12748938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718769-T-C

12748939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718770-G-T

http://identifiers.org/hco/3/GRCh38#12749345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115718878-C-A

12749396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718930-A-T

12749435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115718967-T-C

12749562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719094-T-A

12749562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719094-T-C

12749640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115719156-T-A

12749640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115719156-T-G

12749662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719177-T-A

12749662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719177-T-G

12749663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719178-G-A

12749663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719178-G-C

12749663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719178-G-T

http://identifiers.org/hco/3/GRCh38#12749690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115719207-C-A

12749706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719222-T-C

12749731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719244-G-A

12749731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719244-G-T

12749821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: synonymous variant
orthologous variants: 115719329-T-C

12749821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: synonymous variant
orthologous variants: 115719329-T-G

http://identifiers.org/hco/3/GRCh38#12749968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115719477-A-C

12749968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115719477-A-G

12758485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735342-A-G

http://identifiers.org/hco/3/GRCh38#12758486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115735343-C-A

12758486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735343-C-G

12758486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735343-C-T

http://identifiers.org/hco/3/GRCh38#12758531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115735403-C-A

12758868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735572-T-C

12759011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735701-T-A

12759145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735841-A-G

12759148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735848-T-C

12759149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115735849-G-T

http://identifiers.org/hco/3/GRCh38#12759166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115735867-C-A

12759166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115735867-C-T

12759179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115735880-A-G

12759256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 115735960-G-A

http://identifiers.org/hco/3/GRCh38#12759580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#115736283-C-A

12759580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115736283-C-G

http://identifiers.org/hco/3/GRCh38#12759583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#115736286-C-A

12759609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115736308-G-A

12759609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115736308-G-T

12759858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115736565-C-T

12760052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115736723-C-T

12760171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115736842-T-C

12760171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115736842-T-G

http://identifiers.org/hco/3/GRCh38#12760364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115736994-A-C

12760633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115737215-T-C

12763244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115737863-C-T

12763344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115737975-T-C

12763379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115737990-G-A

12763399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115738009-T-G

12763445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115738058-G-A

12763609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115738211-G-C

12763613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115738215-G-A

12763689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron_variant, undefined
orthologous variants: 115738295-C-G

12763817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115738400-C-T

12764435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115738874-T-A

12764435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115738874-T-C

12764435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115738874-T-G

12766854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115739867-A-G

12767222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115740366-C-G

12767222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115740366-C-T

12767312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115740504-C-T

12767524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115740973-A-T

12767657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115741088-C-G

12767721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115741144-T-C

http://identifiers.org/hco/3/GRCh38#12767730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#115741151-C-A

12767820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115741208-T-C

12767865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25620
most severe consequence: intron variant
orthologous variants: 115741251-G-C